Granulomatous disease, chronic, autosomal dominant type

Preferred Label : Granulomatous disease, chronic, autosomal dominant type;

Obsolete resource : true;

Moved to : 306400;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant form;

Prefixed ID : 138990;

Details

Origin ID

138990;

UMLS CUI

C1841825;

Currated CISMeF NLP mapping
- granulomatous disease, chronic, autosomal dominant type [MeSH concept]
- granulomatous disease, chronic, autosomal dominant type [MeSH Supplementary Concept]
HPO term(s)
- Usually autosomal dominant [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- granulomatous disease, chronic, autosomal dominant type [MeSH Supplementary Concept]
- granulomatous disease, chronic, autosomal dominant type [MeSH concept]

Keyword's position in hierarchy(ies) :

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