Agent Commons Collaborative Research
Congenital analbuminemia
rareCongenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA).
- Identifiers
- MONDO:0014449 OMIM:616000Orphanet:86816
- Causal genes
- ALB
- Also known as
- ANALBA · analbuminemia
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