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X-linked intellectual disability, Hedera type
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
X-linked parkinsonism-spasticity syndrome
Renal tubular dysgenesis of genetic origin
Hyperuricemia - anemia - renal failure
Acute promyelocytic leukemia
Hereditary combined deficiency of vitamin K-dependent clotting factors
Synonym(s):
- MRXSH
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ATP6AP2 O75787300556
No signs/symptoms info available.