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Hereditary central diabetes insipidus
2 OMIM references -
1 associated gene
7 connected diseases
10 signs/symptoms
Disease Type of connection
Alpha-crystallinopathy
Familial isolated dilated cardiomyopathy
Fatal infantile hypertonic myofibrillar myopathy
Posterior polar cataract
Zonular cataract
Nephrogenic diabetes insipidus
Nephrogenic syndrome of inappropriate antidiuresis
Synonym(s):
- Hereditary CDI
- Hereditary neurogenic diabetes insipidus
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
AVP P01185192340
Very frequent
- Diabetes insipidus
- Pollakiuria / polyuria / dysuria / anuria / acute urine retention / oliguria
- Thirst

Frequent
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Fever / chilling
- Humour troubles / anxiety / depression / apathy / euphoria / irritability
- Malabsorption / chronic diarrhea / steatorrhea
- Nausea / vomiting / regurgitation / merycism / hyperemesis
- Obnubilation / coma / lethargia / desorientation
- Weight loss / loss of appetite / break in weight curve / general health alteration