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Dent disease type 2
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Oculocerebrorenal syndrome
Inflammatory myofibroblastic tumor
Translocation renal cell carcinoma
Papillary or follicular thyroid carcinoma
Donnai-Barrow syndrome
Synonym(s):
- Nephrolithiasis type 2
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
OCRL Q01968300535
No signs/symptoms info available.