Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandCafe-au-Lait Spots (D019080)
Parent Node:
expandHypertelorism (D006972)
Parent Node:
expandMyopia (D009216)
Parent Node:
expandPeptic Ulcer (D010437)
..Starting node
..expandGastrocutaneous syndrome (C535651)

       Child Nodes:



 Sister Nodes: 
..expandDuodenal Ulcer (D004381) Child3
..expandEsophagitis, Peptic (D004942)
..expandGastrocutaneous syndrome (C535651)
..expandPeptic Ulcer Perforation (D010439)
..expandStomach Ulcer (D013276)
..expandZollinger-Ellison Syndrome (D015043)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:4520
Name:Gastrocutaneous syndrome
Definition:
Alternative IDs:
ParentIDs:MESH:D006972|MESH:D009216|MESH:D010437|MESH:D019080
TreeNumbers:C05.116.099.370.231.480/C535651 |C05.660.207.231.480/C535651 |C06.405.469.275.800/C535651 |C06.405.608/C535651 |C06.405.748.586/C535651 |C11.744.636/C535651 |C16.131.621.207.231.480/C535651 |C17.800.621.250/C535651 |C23.888.885.250/C535651
Synonyms:
Slim Mappings:Congenital abnormality|Digestive system disease|Eye disease|Musculoskeletal disease|Signs and symptoms|Skin disease
Reference: MedGen: C535651
MeSH: C535651
OMIM: 137270;

Genes:
Phenotypes
1 HP:0000006Autosomal dominant inheritance
2 HP:0000957Cafe-au-lait spot
3 HP:0002036Hiatus hernia
4 HP:0000316Hypertelorism
5 HP:0001003Multiple lentigines
6 HP:0000545Myopia
7 HP:0004398Peptic ulcer
Disease Causing ClinVar Variants