nephrogenic syndrome of inappropriate antidiuresis

Preferred Label : nephrogenic syndrome of inappropriate antidiuresis;

MeSH note : mutation in AVPR2;

Origin ID

C564491;

UMLS CUI

C1845202;

Automatic exact mappings (from CISMeF team)
- Inappropriate antidiuretic hormone secretion syndrome [ORDO Disease]
- Syndrome of Inappropriate Antidiuretic Hormone Secretion [NCIt concept]
- Syndrome of inappropriate secretion of antidiuretic hormone [ICD-11 Subcategory]
- Syndrome of inappropriate vasopressin secretion (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Nephrogenic syndrome of inappropriate antidiuresis [ICD-11 Sub-sub category]
- Nephrogenic syndrome of inappropriate antidiuresis [OMIM Phenotype]
- Nephrogenic syndrome of inappropriate antidiuresis [ORDO Disease]
- Nephrogenic syndrome of inappropriate antidiuresis (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- inappropriate adh syndrome [MeSH Descriptor]
Record concept(s)
- nephrogenic syndrome of inappropriate antidiuresis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Nephrogenic syndrome of inappropriate antidiuresis [OMIM Phenotype]
- Nephrogenic syndrome of inappropriate antidiuresis [ORDO Disease]
- Nephrogenic syndrome of inappropriate antidiuresis (disorder) [SNOMED CT concept]
- nephrogenic syndrome of inappropriate antidiuresis [DO Concept]