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Neurohypophyseal Diabetes Insipidus (MONDO:0007450)

Hereditary central diabetes insipidus is a rare genetic subtype of central diabetes insipidus (CDI) characterized by polyuria and polydipsia due to a deficiency in vasopressin (AVP) synthesis.

Overview

Category

urinary system disorder

reproductive system disorder

nervous system disorder

endocrine system disorder

Ontology ID

MONDO:0007450

Internal:8840

Synonyms

ADH deficiency

AVP deficiency

Arginine vasopressin deficiency

antidiuretic hormone deficiency

diabetes insipidus of pituitary gland

hereditary CDI

hereditary neurogenic diabetes insipidus

pituitary gland diabetes insipidus

vasopressin deficiency

diabetes insipidus, cranial type

diabetes insipidus, neurohypophyseal

diabetes insipidus, primary central

hereditary central diabetes insipidus

neurogenic diabetes insipidus

Mapped terms

DOID:12388

GARD:0016629

MEDGEN:574999

NANDO:2201050

NCIT:C84933

OMIM:125700

Orphanet:30925

SCTID:45369008

UMLS:C0342394

icd11.foundation:97299603

Child terms

Unknown children.

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