Autosomal Dominant Neurohypophyseal Diabetes Insipidus

Preferred Label : Autosomal Dominant Neurohypophyseal Diabetes Insipidus;

NCIt related terms : ADNDI;

NCIt definition : An autosomal dominant form of diabetes insipidus caused by mutation(s) in the AVP gene encoding arginine vasopressin.;

NCI Metathesaurus CUI : CL513021;

Details

Origin ID

C129736;

UMLS CUI

C4331824;

CISMeF manual mappings
- autosomal dominant neurogenic diabetes insipidus [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- autosomal dominant neurogenic diabetes insipidus [Disease (Nov.)]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]
disease_mapped_to_gene
- AVP Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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