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1 OMIM reference -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Renal tubular dysgenesis of genetic origin
Autosomal recessive Emery-Dreifuss muscular dystrophy

ACE LMNA
AGT
AGTR1
REN


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ACE
(0.49)
LMNA



Citations in the biomedical literature:


Renal tubular dysgenesis of genetic origin
ACE AGT AGTR1 REN
Autosomal recessive Emery-Dreifuss muscular dystrophy
LMNA



Renal tubular dysgenesis of genetic origin
Autosomal recessive Emery-Dreifuss muscular dystrophy

Synonym(s):
(no synonyms)

Synonym(s):
- EDMD3

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D020389

No signs/symptoms info available.