ONTOLOGY REPORT - ANNOTATIONS

Term:Fetal Diseases
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Accession:RDO:0001592 term browser browse the term
Definition:Pathophysiological conditions of the FETUS in the UTERUS. Some fetal diseases may be treated with FETAL THERAPIES.
Synonyms:exact_synonym: Embryopathies;   Embryopathy;   Fetal Disease
 primary_id: MESH:D005315

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Fetal Diseases term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Nos2 nitric oxide synthase 2, inducible GBrowse link ISS 10 65,036,884 65,072,453 RGD:2313217 RGD
G Prkcb protein kinase C, beta GBrowse link IEP 1 181,117,512 181,459,856 RGD:1625524 RGD
Bowen-Conradi syndrome term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Emg1 EMG1 N1-specific pseudouridine methyltransferase GBrowse link ISS 4 160,826,925 160,835,206 RGD:7240710 OMIM
Chorioamnionitis term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Ager advanced glycosylation end product-specific receptor GBrowse link ISS 20 4,250,613 4,253,540 RGD:6767308 RGD
G Il6 interleukin 6 GBrowse link ISS 4 456,799 461,376 RGD:5128667 RGD
G Tgfb1 transforming growth factor, beta 1 GBrowse link Severity ISS 1 80,894,705 80,911,020 RGD:4145137 RGD
COCOON SYNDROME term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Chuk conserved helix-loop-helix ubiquitous kinase GBrowse link ISS 1 249,122,845 249,158,369 RGD:7240710 OMIM
Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Ptf1a pancreas specific transcription factor, 1a GBrowse link ISS 17 93,494,689 93,496,543 RGD:7240710 OMIM
Fetal Alcohol Syndrome term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Rhoa ras homolog family member A IEP RGD:2298867 RGD
Fetal Growth Retardation term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Agtr1a angiotensin II receptor, type 1a GBrowse link IEP 17 40,629,318 40,684,982 RGD:5129179 RGD
G Agtr2 angiotensin II receptor, type 2 IEP RGD:5129179 RGD
G Cad carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase GBrowse link IEP 6 25,272,416 25,296,266 RGD:2303532 RGD
G Cps1 carbamoyl-phosphate synthetase 1 GBrowse link IEP 9 65,907,211 66,017,942 RGD:2303532 RGD
G Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 GBrowse link IEP 8 61,793,976 61,805,308 RGD:4832477 RGD
G Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 GBrowse link IEP 7 112,977,395 112,984,080 RGD:4891147 RGD
G Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 GBrowse link IEP 7 113,043,365 113,049,779 RGD:4891147 RGD
G Dusp5 dual specificity phosphatase 5 GBrowse link IEP 1 259,754,234 259,767,645 RGD:2317872 RGD
G G6pc glucose-6-phosphatase, catalytic subunit GBrowse link IEP 10 90,393,531 90,403,485 RGD:2315963 RGD
G Gria1 glutamate receptor, ionotropic, AMPA 1 GBrowse link IEP 10 42,613,359 42,616,610 RGD:4107070 RGD
G Grin2a glutamate receptor, ionotropic, N-methyl D-aspartate 2A GBrowse link IEP 10 5,588,229 6,004,780 RGD:4107070 RGD
G Hadha hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit GBrowse link IEP 6 26,173,798 26,191,433 RGD:1599884 RGD
G Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 GBrowse link IEP 19 35,336,342 35,341,585 RGD:2308941 RGD
G Igf1 insulin-like growth factor 1 GBrowse link IEP 7 24,531,669 24,605,742 RGD:2306715 RGD
G Igf1r insulin-like growth factor 1 receptor GBrowse link ISS 1 122,704,976 122,990,007 RGD:1624299 RGD
G Il1a interleukin 1 alpha GBrowse link ISS 3 116,913,612 116,924,114 RGD:2311066 RGD
G Lct lactase GBrowse link IED 13 40,990,315 41,043,388 RGD:1600258 RGD
G Lep leptin GBrowse link IED 4 55,943,837 55,945,938 RGD:5128507 RGD
G Mdm2 p53 E3 ubiquitin protein ligase GBrowse link IEP 7 56,996,694 57,020,926 RGD:2317395 RGD
G Nos1 nitric oxide synthase 1, neuronal GBrowse link IEP 12 39,812,500 39,869,484 RGD:5132592 RGD
G Nos2 nitric oxide synthase 2, inducible GBrowse link IEP 10 65,036,884 65,072,453 RGD:5132592 RGD
G Nos3 nitric oxide synthase 3, endothelial cell GBrowse link IEP 4 6,158,847 6,179,441 RGD:5132592 RGD
G Nr3c1 nuclear receptor subfamily 3, group C, member 1 GBrowse link IED 18 32,371,496 32,459,145 RGD:4892120 RGD
G Nr3c1 nuclear receptor subfamily 3, group C, member 1 GBrowse link IEP 18 32,371,496 32,459,145 RGD:2308941 RGD
G Otc ornithine carbamoyltransferase GBrowse link IEP X 24,609,141 24,685,341 RGD:4144077 RGD
G Pdgfa platelet-derived growth factor alpha polypeptide GBrowse link ISS 12 16,151,045 16,172,412 RGD:2311066 RGD
G Pdgfb platelet-derived growth factor beta polypeptide GBrowse link ISS 7 118,244,385 118,262,021 RGD:2311066 RGD
G Pdx1 pancreatic and duodenal homeobox 1 IEP RGD:2311220 RGD
G Ptgs2 prostaglandin-endoperoxide synthase 2 GBrowse link IEP 13 64,427,288 64,432,978 RGD:2308941 RGD
G Slc2a1 solute carrier family 2 (facilitated glucose transporter), member 1 GBrowse link IEP 5 139,690,801 139,719,021 RGD:730192 RGD
G Slc2a3 solute carrier family 2 (facilitated glucose transporter), member 3 GBrowse link IEP 4 159,210,116 159,221,169 RGD:730192 RGD
G Srebf1 sterol regulatory element binding transcription factor 1 GBrowse link IEP 10 46,461,684 46,483,646 RGD:2308805 RGD
G Srebf1_v2 sterol regulatory element binding factor 1, variant 2 IEP RGD:2308805 RGD
G Star steroidogenic acute regulatory protein GBrowse link IEP 16 70,642,580 70,647,203 RGD:4832477 RGD
G Unc13a unc-13 homolog A (C. elegans) GBrowse link IEP 16 18,827,405 18,872,461 RGD:5686390 RGD
Fetal Hypoxia term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Crh corticotropin releasing hormone GBrowse link IEP 2 104,764,023 104,765,887 RGD:5491006 RGD
G Crhr1 corticotropin releasing hormone receptor 1 GBrowse link IEP 10 93,312,405 93,354,229 RGD:5491006 RGD
G Crhr2 corticotropin releasing hormone receptor 2 GBrowse link IEP 4 83,839,822 83,867,017 RGD:5491006 RGD
G Mmp1 matrix metallopeptidase 1 (interstitial collagenase) GBrowse link IEP 8 4,333,773 4,354,284 RGD:7207283 RGD
G Mmp13 matrix metallopeptidase 13 GBrowse link IEP 8 4,158,887 4,169,166 RGD:7207283 RGD
G Nos1 nitric oxide synthase 1, neuronal GBrowse link IEP 12 39,812,500 39,869,484 RGD:1642145 RGD
Fetal Macrosomia term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Lipc lipase, hepatic GBrowse link IEP 8 75,323,442 75,450,353 RGD:2308786 RGD
Finnish lethal neonatal metabolic syndrome term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Bcs1l BC1 (ubiquinol-cytochrome c reductase) synthesis-like GBrowse link ISS 9 73,939,024 73,943,055 RGD:7240710 OMIM
Hydrops Fetalis term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Sftpa1 surfactant protein A1 GBrowse link ISS 16 17,570,887 17,574,389 RGD:4143453 RGD
HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Lbr lamin B receptor GBrowse link ISS 13 97,814,439 97,834,860 RGD:7240710 OMIM
Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Cdkn1c cyclin-dependent kinase inhibitor 1C GBrowse link ISS 1 203,835,215 203,837,844 RGD:7240710 OMIM
Kernicterus term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
S ACI/N-j TAS RGD:1302917 RGD
Meconium Aspiration Syndrome term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Scgb1a1 secretoglobin, family 1A, member 1 (uteroglobin) GBrowse link ISS 1 211,758,103 211,761,651 RGD:5144123 RGD
Microcephalic Osteodysplastic Primordial Dwarfism, Type II term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Pcnt pericentrin GBrowse link ISS 20 12,608,650 12,694,390 RGD:7240710 OMIM
MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Chrna1 cholinergic receptor, nicotinic, alpha 1 (muscle) GBrowse link ISS 3 56,087,754 56,102,821 RGD:7240710 OMIM
G Chrnd cholinergic receptor, nicotinic, delta (muscle) GBrowse link ISS 9 85,996,421 86,004,839 RGD:7240710 OMIM
G Chrng cholinergic receptor, nicotinic, gamma (muscle) GBrowse link ISS 9 86,012,089 86,018,199 RGD:7240710 OMIM
SECKEL SYNDROME 4 term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Cenpj centromere protein J GBrowse link ISS 15 35,487,198 35,550,034 RGD:7240710 OMIM
Term paths to the root
Path 1
Term Annotations click to browse term
  Diseases 30711
    Congenital, Hereditary, and Neonatal Diseases and Abnormalities 3912
      Fetal Diseases 62
        COCOON SYNDROME 1
        Chorioamnionitis 3
        Echogenic Bowel 0
        Erythroblastosis, Fetal + 3
        Fetal Alcohol Syndrome + 1
        Fetal Growth Retardation + 41
        Fetal Hypoxia 6
        Fetal Macrosomia + 1
        Fetal Nutrition Disorders 0
        MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE 3
        Meconium Aspiration Syndrome 1
        Megaduodenum 0
        Nuchal Cord 0
        Pyelectasis 0
Path 2
Term Annotations click to browse term
  Diseases 30711
    Female Urogenital Diseases and Pregnancy Complications 4218
      Pregnancy Complications 205
        Fetal Diseases 62
          COCOON SYNDROME 1
          Chorioamnionitis 3
          Echogenic Bowel 0
          Erythroblastosis, Fetal + 3
          Fetal Alcohol Syndrome + 1
          Fetal Growth Retardation + 41
          Fetal Hypoxia 6
          Fetal Macrosomia + 1
          Fetal Nutrition Disorders 0
          MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE 3
          Meconium Aspiration Syndrome 1
          Megaduodenum 0
          Nuchal Cord 0
          Pyelectasis 0
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