ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

COMMON GENES: 2
PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Autosomal recessive Alport syndrome

Autosomal dominant Alport syndrome

COL4A3	(UniProt - OMIM)		COL4A3	(UniProt - OMIM)
COL4A4	(UniProt - OMIM)		COL4A4	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL4A3	(0.52)	COL4A4

Citations in the biomedical literature:

Autosomal recessive Alport syndrome		Autosomal dominant Alport syndrome

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare otorhinolaryngologic disease - Rare renal disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare otorhinolaryngologic disease - Rare renal disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: - Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: - 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 - 1 MeSH reference: C536586

No signs/symptoms info available.