Cytoscape Web
Click node...

Idiopathic hypercalciuria
2 OMIM references -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Combined immunodeficiency due to STK4 deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
ADCY10 Q96PN6605205
No signs/symptoms info available.