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Neurohypophyseal diabetes insipidus
rareHereditary 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.
- Identifiers
- MONDO:0007450 OMIM:125700Orphanet:30925
- Causal genes
- AVP
- Part of
- Autosomal dominant diseaseCentral diabetes insipidusDiabetes insipidusHereditary neurological diseaseInherited kidney disorderPituitary gland disorder
- Also known as
- ADH deficiency · antidiuretic hormone deficiency · Arginine Vasopressin Deficiency · AVP deficiency · diabetes insipidus of pituitary gland
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