Alport syndrome 3b, autosomal recessive

Preferred Label : Alport syndrome 3b, autosomal recessive;

Symbol : ATS3B;

Type : Phenotype, molecular basis known;

Prefixed ID : #620536;

Details

Origin ID

620536;

UMLS CUI

C5882699;

Genes related to phenotype
- Collagen, type iv, alpha-3 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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