Gene: Col1a2 (collagen type I alpha 2 chain) Rattus norvegicus
Analyze
Symbol:
Col1a2
Name:
collagen type I alpha 2 chain
Description:
Predicted to have several functions, including identical protein binding activity; platelet-derived growth factor binding activity; and protease binding activity. Involved in cellular response to retinoic acid; cellular response to thyroid hormone stimulus; and response to norepinephrine. Predicted to localize to collagen type I trimer; endoplasmic reticulum; and extracellular space. Biomarker of hypothyroidism; muscular atrophy; pulmonary fibrosis; and ureteral obstruction. Human ortholog(s) of this gene implicated in Ehlers-Danlos syndrome; heart valve disease; intracranial aneurysm; osteogenesis imperfecta (multiple); and osteoporosis. Orthologous to human COL1A2 (collagen type I alpha 2 chain); PARTICIPATES IN endothelin signaling pathway; interleukin-4 signaling pathway; syndecan signaling pathway; INTERACTS WITH 1-naphthyl isothiocyanate; 17alpha-ethynylestradiol; 2,3,7,8-tetrachlorodibenzodioxine.
Type:
protein-coding
RefSeq Status:
PROVISIONAL
Also known as:
alpha-2 type I collagen; collagen alpha-2(I) chain; collagen, type I, alpha 2; procollagen, type I, alpha 2
Orthologs:
Species
Gene symbol and name
Data Source
Assertion derived from
less info ...
Orthologs 1
Homo sapiens (human):
COL1A2 (collagen type I alpha 2 chain) HGNC
Ensembl, HomoloGene, Inparanoid, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Mus musculus (house mouse):
Col1a2 (collagen, type I, alpha 2) HGNC
Treefam, OrthoMCL, OMA, HomoloGene, Inparanoid, Panther, OrthoDB, Ensembl
Chinchilla lanigera (long-tailed chinchilla):
Col1a2 (collagen type I alpha 2 chain) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Pan paniscus (bonobo/pygmy chimpanzee):
COL1A2 (collagen type I alpha 2 chain) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Canis lupus familiaris (dog):
COL1A2 (collagen type I alpha 2 chain) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):
Col1a2 (collagen type I alpha 2 chain) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Sus scrofa (pig):
COL1A2 (collagen type I alpha 2 chain) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Chlorocebus sabaeus (African green monkey):
COL1A2 (collagen type I alpha 2 chain) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Heterocephalus glaber (naked mole-rat):
Col1a2 (collagen type I alpha 2 chain) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Other homologs 2
Homo sapiens (human):
COL5A1 (collagen type V alpha 1 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL2A1 (collagen type II alpha 1 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL1A1 (collagen type I alpha 1 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL11A1 (collagen type XI alpha 1 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL5A3 (collagen type V alpha 3 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL4A3 (collagen type IV alpha 3 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL5A2 (collagen type V alpha 2 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL3A1 (collagen type III alpha 1 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL4A4 (collagen type IV alpha 4 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL4A1 (collagen type IV alpha 1 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL4A2 (collagen type IV alpha 2 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL22A1 (collagen type XXII alpha 1 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL16A1 (collagen type XVI alpha 1 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL7A1 (collagen type VII alpha 1 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL4A6 (collagen type IV alpha 6 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL24A1 (collagen type XXIV alpha 1 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL11A2 (collagen type XI alpha 2 chain) HGNC
OrthoMCL
Homo sapiens (human):
COL4A5 (collagen type IV alpha 5 chain) HGNC
OrthoMCL
Alliance orthologs 3
Homo sapiens (human):
COL1A2 (collagen type I alpha 2 chain)
Alliance
DIOPT (Ensembl Compara|InParanoid|PhylomeDB|PANTHER|OrthoFinder|HGNC|OrthoInspector|Hieranoid)
Mus musculus (house mouse):
Col1a2 (collagen, type I, alpha 2)
Alliance
DIOPT (Ensembl Compara|InParanoid|PhylomeDB|PANTHER|OrthoFinder|OrthoInspector|Hieranoid)
Latest Assembly:
Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl Rnor_6.0 4 31,534,225 - 31,569,152 (+) NCBI Rnor6.0 Rnor_6.0 rn6 Rnor6.0 Rnor_6.0 Ensembl 4 31,534,225 - 31,569,151 (+) Ensembl Rnor6.0 rn6 Rnor6.0 Rnor_5.0 4 31,405,253 - 31,440,180 (+) NCBI Rnor5.0 Rnor_5.0 rn5 Rnor5.0 Rnor_5.0 4 29,442,828 - 29,478,616 (+) NCBI Rnor5.0 Rnor_5.0 rn5 Rnor5.0 RGSC_v3.4 4 29,393,645 - 29,428,572 (+) NCBI RGSC3.4 rn4 RGSC3.4 RGSC_v3.1 4 29,431,383 - 29,467,014 (+) NCBI Celera 4 27,947,892 - 27,982,658 (+) NCBI Celera Cytogenetic Map 4 q21 NCBI
JBrowse:
View Region in Genome Browser (JBrowse)
Model
Disease Annotations
Imported Annotations - ClinVar
ARTERIAL DISSECTION ISO RGD:730984 8554872 ClinVar Annotator: match by term: Predisposition to dissection ClinVar PMID:25741868 , PMID:28492532 bone development disease ISO RGD:730984 8554872 ClinVar Annotator: match by term: Skeletal dysplasia ClinVar PMID:25741868 connective tissue disease ISO RGD:730984 8554872 ClinVar Annotator: match by term: Connective tissue disorder ClinVar PMID:25741868 connective tissue disease ISO RGD:730984 8554872 ClinVar Annotator: match by term: Connective tissue disorder ClinVar PMID:25741868 more ... connective tissue disease ISO RGD:730984 8554872 ClinVar Annotator: match by term: Connective tissue disorder ClinVar PMID:15172002 more ... connective tissue disease ISO RGD:730984 8554872 ClinVar Annotator: match by term: Connective tissue disorder ClinVar PMID:25741868 , PMID:28492532 dentinogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Dentinogenesis imperfecta ClinVar PMID:26788535 Ehlers-Danlos Syndrome Type 7 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, procollagen proteinase deficient ClinVar PMID:24033266 more ... Ehlers-Danlos Syndrome Type 7 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, procollagen proteinase deficient ClinVar PMID:26467025 Ehlers-Danlos Syndrome Type 7 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, procollagen proteinase deficient ClinVar PMID:18272325 more ... Ehlers-Danlos Syndrome Type 7 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, procollagen proteinase deficient ClinVar PMID:25741868 , PMID:26467025 Ehlers-Danlos Syndrome Type 7 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, procollagen proteinase deficient ClinVar PMID:26467025 , PMID:28492532 Ehlers-Danlos Syndrome Type 7 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, procollagen proteinase deficient ClinVar PMID:18996919 , PMID:28492532 Ehlers-Danlos Syndrome Type 7 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, procollagen proteinase deficient ClinVar Ehlers-Danlos Syndrome Type 7 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, procollagen proteinase deficient ClinVar PMID:28492532 Ehlers-Danlos Syndrome Type 7 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, procollagen proteinase deficient ClinVar PMID:25741868 , PMID:28492532 Ehlers-Danlos Syndrome Type 7 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, procollagen proteinase deficient ClinVar PMID:10976985 more ... Ehlers-Danlos Syndrome Type 7 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, procollagen proteinase deficient ClinVar PMID:25741868 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome arthrochalasia type ClinVar PMID:25741868 , PMID:26467025 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome arthrochalasia type ClinVar PMID:10976985 more ... EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome arthrochalasia type ClinVar PMID:24033266 more ... EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome arthrochalasia type ClinVar PMID:26467025 , PMID:28492532 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome arthrochalasia type ClinVar PMID:18272325 more ... EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome arthrochalasia type ClinVar PMID:18996919 , PMID:28492532 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:130060 ClinVar PMID:25741868 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:130060 ClinVar EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome arthrochalasia type ClinVar PMID:25741868 , PMID:28492532 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome arthrochalasia type ClinVar PMID:26467025 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome arthrochalasia type ClinVar PMID:28492532 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:25741868 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ClinVar PMID:25741868 , PMID:31319225 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:25741868 more ... EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:21520333 more ... EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:17078022 more ... EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:11288717 more ... EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:1577745 more ... EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:2454224 more ... EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:1556139 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ClinVar PMID:25741868 , PMID:28492532 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:2777808 , PMID:4742738 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:2993307 EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:16705691 more ... EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT ClinVar PMID:16705691 more ... Ehlers-Danlos Syndrome, Cardiac Valvular Form ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form ClinVar PMID:25741868 more ... Ehlers-Danlos Syndrome, Cardiac Valvular Form ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form ClinVar PMID:17078022 more ... Ehlers-Danlos Syndrome, Cardiac Valvular Form ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form ClinVar PMID:21520333 more ... Ehlers-Danlos Syndrome, Cardiac Valvular Form ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form ClinVar PMID:28492532 Ehlers-Danlos Syndrome, Cardiac Valvular Form ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form ClinVar PMID:15077201 more ... Ehlers-Danlos Syndrome, Cardiac Valvular Form ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form ClinVar PMID:16816023 Ehlers-Danlos Syndrome, Cardiac Valvular Form ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form ClinVar PMID:16705691 more ... Ehlers-Danlos Syndrome, Cardiac Valvular Form ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form ClinVar PMID:25741868 , PMID:28492532 Ehlers-Danlos Syndrome, Cardiac Valvular Form ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form ClinVar PMID:16705691 more ... Ehlers-Danlos Syndrome, Cardiac Valvular Form ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form ClinVar PMID:15077201 , PMID:9295084 Ehlers-Danlos Syndrome, Cardiac Valvular Form ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:225320 ClinVar PMID:15077201 genetic disease ISO RGD:730984 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar genetic disease ISO RGD:730984 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:15077201 more ... genetic disease ISO RGD:730984 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:15077201 more ... genetic disease ISO RGD:730984 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:15077201 more ... genetic disease ISO RGD:730984 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:10027910 more ... Marfan syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Marfan syndrome, atypical ClinVar PMID:15172002 more ... myoclonic dystonia ISO RGD:730984 8554872 ClinVar Annotator: match by term: Myoclonic dystonia ClinVar PMID:23677909 , PMID:28492532 osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta ClinVar PMID:26467025 , PMID:28492532 osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta ClinVar PMID:25741868 osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Lobstein's Disease ClinVar PMID:11288717 more ... osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Lobstein's Disease ClinVar PMID:25741868 more ... osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Lobstein's Disease ClinVar PMID:17078022 more ... osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Lobstein's Disease ClinVar PMID:21520333 more ... osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta ClinVar PMID:24767406 more ... osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Lobstein's Disease ClinVar PMID:16705691 more ... osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Lobstein's Disease ClinVar PMID:25326637 , PMID:28492532 osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta ClinVar PMID:15077201 more ... osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta ClinVar PMID:17078022 more ... osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Lobstein's Disease ClinVar PMID:23692737 , PMID:28492532 osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Lobstein's Disease ClinVar PMID:25944380 , PMID:28492532 osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta ClinVar PMID:18996919 , PMID:28492532 osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta ClinVar PMID:11317364 osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Lobstein's Disease ClinVar osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Lobstein disease ClinVar PMID:16705691 more ... osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta, mild ClinVar PMID:3403536 osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Lobstein's Disease ClinVar PMID:25741868 , PMID:28492532 osteogenesis imperfecta ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta ClinVar PMID:28492532 osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type 1 with dentinogenesis imperfecta ClinVar PMID:18996919 , PMID:28492532 osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:17078022 more ... osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:11288717 more ... osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:25741868 more ... osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:17078022 more ... osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:21520333 more ... osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:16705691 more ... osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:25741868 osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:25944380 , PMID:28492532 osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:25326637 , PMID:28492532 osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:23692737 , PMID:28492532 osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:28492532 osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:25741868 , PMID:28492532 osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:17078022 more ... osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:25944380 osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:16879195 more ... osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:11317364 more ... osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type 1 with dentinogenesis imperfecta ClinVar PMID:16705691 more ... osteogenesis imperfecta type 1 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type I ClinVar PMID:26467025 , PMID:28492532 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166210 ClinVar PMID:1874719 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA ClinVar PMID:25741868 more ... osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA ClinVar PMID:17078022 more ... osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA ClinVar PMID:21520333 more ... osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA ClinVar PMID:28492532 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA ClinVar PMID:16705691 more ... osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IIA ClinVar PMID:25326637 , PMID:28492532 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: OSTEOGENESIS IMPERFECTA, TYPE II ClinVar PMID:3372533 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: OSTEOGENESIS IMPERFECTA, TYPE II ClinVar PMID:1385413 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Vrolik type of osteogenesis imperfecta ClinVar PMID:16705691 more ... osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166210 ClinVar PMID:25741868 , PMID:26938784 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by term: OI, TYPE II ClinVar PMID:25741868 , PMID:28492532 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166210 ClinVar PMID:2839839 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166210 ClinVar PMID:1711048 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166210 ClinVar PMID:1301191 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166210 ClinVar PMID:9923651 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166210 ClinVar PMID:2914942 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166210 ClinVar PMID:7959683 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166210 ClinVar PMID:2777764 osteogenesis imperfecta type 2 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166210 ClinVar osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:259420 ClinVar PMID:8444468 osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:17078022 more ... osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:25741868 more ... osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:17078022 more ... osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:21520333 more ... osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:25326635 , PMID:25741868 osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:16705691 more ... osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:25326637 , PMID:28492532 osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:25741868 osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:2824475 osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:3023615 more ... osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: OI type III ClinVar PMID:16705691 more ... osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:25741868 , PMID:28492532 osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:25944380 osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:259420 ClinVar osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis imperfecta type III ClinVar PMID:25741868 more ... osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:259420 ClinVar PMID:6092353 osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:259420 ClinVar PMID:10807697 osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:259420 ClinVar PMID:19208385 osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:259420 ClinVar PMID:19208385 more ... osteogenesis imperfecta type 3 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:259420 ClinVar PMID:2064612 more ... osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166220 ClinVar PMID:2064612 more ... osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IV ClinVar PMID:25741868 osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IV ClinVar PMID:11288717 more ... osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IV ClinVar PMID:25741868 more ... osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IV ClinVar PMID:17078022 more ... osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IV ClinVar PMID:21520333 more ... osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IV ClinVar PMID:16705691 more ... osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IV ClinVar PMID:25326637 , PMID:28492532 osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IV ClinVar PMID:25944380 , PMID:28492532 osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by term: OI type IV ClinVar PMID:16705691 more ... osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IV ClinVar PMID:25741868 , PMID:28492532 osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by term: Osteogenesis Imperfecta Type IV ClinVar PMID:25944380 osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166220 ClinVar osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166220 ClinVar PMID:8829655 osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166220 ClinVar PMID:8456807 osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166220 ClinVar PMID:8786065 osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166220 ClinVar PMID:9268111 osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166220 ClinVar PMID:11836364 osteogenesis imperfecta type 4 ISO RGD:730984 8554872 ClinVar Annotator: match by OMIM:166220 ClinVar PMID:2897363 osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: OSTEOPOROSIS, INVOLUTIONAL ClinVar PMID:25741868 more ... osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: OSTEOPOROSIS, INVOLUTIONAL ClinVar PMID:17078022 more ... osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: OSTEOPOROSIS, INVOLUTIONAL ClinVar PMID:21520333 more ... osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: OSTEOPOROSIS, INVOLUTIONAL ClinVar PMID:16705691 more ... osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: OSTEOPOROSIS, INVOLUTIONAL ClinVar PMID:25741868 , PMID:28492532 osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: OSTEOPOROSIS, INVOLUTIONAL ClinVar PMID:16705691 more ... pleomorphic xanthoastrocytoma ISO RGD:730984 8554872 ClinVar Annotator: match by term: Pleomorphic xanthoastrocytoma ClinVar PMID:28299358 Postmenopausal Osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: Postmenopausal osteoporosis ClinVar PMID:16705691 more ... Postmenopausal Osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: Postmenopausal osteoporosis ClinVar PMID:25741868 more ... Postmenopausal Osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: Postmenopausal osteoporosis ClinVar PMID:17078022 more ... Postmenopausal Osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: Postmenopausal osteoporosis ClinVar PMID:21520333 more ... Postmenopausal Osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: Postmenopausal osteoporosis ClinVar PMID:1463018 more ... Postmenopausal Osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: Postmenopausal osteoporosis ClinVar PMID:16705691 more ... Postmenopausal Osteoporosis ISO RGD:730984 8554872 ClinVar Annotator: match by term: Postmenopausal osteoporosis ClinVar PMID:25741868 , PMID:28492532 type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 1 ClinVar PMID:28492532 type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:23692737 , PMID:28492532 type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:11288717 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:16705691 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 ClinVar PMID:11288717 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 ClinVar PMID:25741868 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 ClinVar PMID:21520333 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 ClinVar PMID:24033266 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:16816023 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:21520333 , PMID:28492532 type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:15077201 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 ClinVar PMID:16705691 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 1 ClinVar PMID:25326637 , PMID:28492532 type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 1 ClinVar PMID:2454224 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:11359465 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:16786509 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:16879195 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 , PMID:28492532 type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:25741868 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:25146735 , PMID:28492532 type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:16879195 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:11288717 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:11288717 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 1 ClinVar PMID:25944380 , PMID:28492532 type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:10027910 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:18996919 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:11317364 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 ClinVar PMID:16705691 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 ClinVar PMID:26467025 , PMID:28492532 type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 ClinVar PMID:18996919 , PMID:28492532 type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:25289482 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:15241796 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:15172002 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 1 ClinVar PMID:25741868 , PMID:28492532 type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:17078022 more ... type I Ehlers-Danlos syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, classic type ClinVar PMID:25741868 more ... type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:28492532 type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:24033266 more ... type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:11288717 more ... type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:25741868 more ... type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:17078022 more ... type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:21520333 more ... type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:16705691 more ... type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:25326637 , PMID:28492532 type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:23692737 , PMID:28492532 type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:25944380 , PMID:28492532 type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:26467025 , PMID:28492532 type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:16705691 more ... type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:18996919 , PMID:28492532 type II Ehlers-Danlos Syndrome ISO RGD:730984 8554872 ClinVar Annotator: match by term: Ehlers-Danlos syndrome, type 2 ClinVar PMID:25741868 , PMID:28492532
Gene-Chemical Interaction Annotations
