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X-linked intellectual disability, Hedera type
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hyperuricemia - anemia - renal failure
1 OMIM reference -
1 associated gene
No signs/symptoms info
X-linked intellectual disability, Hedera type
Hyperuricemia - anemia - renal failure

ATP6AP2
(UniProt - OMIM)
 REN
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ATP6AP2
(0.78)
REN


Citations in the biomedical literature:


X-linked intellectual disability, Hedera type
ATP6AP2
Hyperuricemia - anemia - renal failure
REN



X-linked intellectual disability, Hedera type
Hyperuricemia - anemia - renal failure

Synonym(s):
- MRXSH
Synonym(s):
- FJHN type 2
- Familial juvenile hyperuricemic nephropathy type 2
- REN-associated FJHN
- REN-associated familial juvenile hyperuricemic nephropathy
- REN-associated kidney disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.