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Renal tubular dysgenesis of genetic origin
1 OMIM reference -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
X-linked intellectual disability, Hedera type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Renal tubular dysgenesis of genetic origin
X-linked intellectual disability, Hedera type

ACE
(UniProt - OMIM)
 ATP6AP2
(UniProt - OMIM)
AGT
(UniProt - OMIM)
AGTR1
(UniProt - OMIM)
REN
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
REN
AGT
(0.78)
(0.52)
ATP6AP2
ATP6AP2


Citations in the biomedical literature:


Renal tubular dysgenesis of genetic origin
ACE AGT AGTR1 REN
X-linked intellectual disability, Hedera type
ATP6AP2



Renal tubular dysgenesis of genetic origin
X-linked intellectual disability, Hedera type

Synonym(s):
(no synonyms)

Synonym(s):
- MRXSH
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.