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Nephrogenic diabetes insipidus
2 OMIM references -
2 associated genes
10 connected diseases
No signs/symptoms info
Disease Type of connection
Nephrogenic syndrome of inappropriate antidiuresis
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Cerebellar ataxia - hypogonadism
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Hereditary central diabetes insipidus
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease

Classification (ICD10):
- Diseases of the genitourinary system -

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
1 MeSH reference: D018500

Gene symbol UniProt reference OMIM reference
AQP2 P41181107777
AVPR2 P30518300538
No signs/symptoms info available.