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Kenny-Caffey syndrome type 2 - Ontology Report - Rat Genome Database

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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:Kenny-Caffey syndrome type 2
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Accession:DOID:0080723 term browser browse the term
Definition:A Kenny-Caffey syndrome that has_material_basis_in heterozygous mutation in the FAM111A gene on chromosome 11q12. (DO)
Synonyms:exact_synonym: KCS2;   Kenny syndrome;   Kenny-Caffey syndrome 2;   autosomal dominant Kenny-Caffey syndrome;   dwarfism, cortical thickening of tubular bones, and transient hypocalcemia
 broad_synonym: FAM111A-RELATED CONDITION
 primary_id: MESH:C537020
 alt_id: MIM:127000
 xref: GARD:83;   MONDO:0007478;   ORDO:93325

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Kenny-Caffey syndrome type 2 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Fam111a FAM111 trypsin like peptidase A ISO ClinVar Annotator: match by term: Autosomal dominant Kenny-Caffey syndrome | ClinVar Annotator: match by term: Dwarfism, cortical thickening of tubular bones and transient hypocalcemia
CTD Direct Evidence: marker/mechanism		 OMIM
ClinVar
CTD		 PMID:23684011 PMID:23996431 PMID:24635597 PMID:24970356 PMID:25741868 More... NCBI chr 1:209,640,865...209,656,551
Ensembl chr 1:209,640,953...209,656,547 		JBrowse link
G Tbce tubulin folding cofactor E ISO CTD Direct Evidence: marker/mechanism CTD PMID:12389028 NCBI chr17:51,290,143...51,336,090
Ensembl chr17:51,290,202...51,336,089 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19140
    syndrome 11403
      Kenny-Caffey syndrome 3
        Kenny-Caffey syndrome type 2 2
Path 2
Term Annotations click to browse term
  disease 19140
    disease of anatomical entity 18453
      Skin and Connective Tissue Diseases 7774
        connective tissue disease 5918
          bone disease 4368
            bone development disease 2387
              osteochondrodysplasia 882
                Caffey disease 5
                  Kenny-Caffey syndrome 3
                    Kenny-Caffey syndrome type 2 2
paths to the root