Gastrocutaneous syndrome

Preferred Label : Gastrocutaneous syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Peptic ulcer/hiatal hernia, multiple lentigines/cafe-au-lait spots, hypertelorism, myopia;

Inheritance : Autosomal dominant;

Prefixed ID : 137270;

Details

Origin ID

137270;

UMLS CUI

C1850899;

Currated CISMeF NLP mapping
- Gastrocutaneous syndrome [ICD-11 More detail]
- Gastrocutaneous syndrome [MeSH concept]
- Gastrocutaneous syndrome [ORDO Disease]
- Gastrocutaneous syndrome (disorder) [SNOMED CT concept]
- gastrocutaneous syndrome [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Cafe-au-lait spot [HPO term]
- Hiatus hernia [HPO term]
- Hypertelorism [HPO term]
- Multiple lentigines [HPO term]
- Myopia [HPO term]
- Peptic ulcer [HPO term]
ORDO concept(s)
- Gastrocutaneous syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Gastrocutaneous syndrome [ORDO Disease]
- Gastrocutaneous syndrome [MeSH concept]
- Gastrocutaneous syndrome (disorder) [SNOMED CT concept]
- gastrocutaneous syndrome [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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