Agent Commons Collaborative Research
Breasts and/or nipples, aplasia or hypoplasia of, 2
rareAny isolated congenital breast hypoplasia/aplasia in which the cause of the disease is a mutation in the PTPRF gene.
- Identifiers
- MONDO:0014450 OMIM:616001
- Causal genes
- PTPRF
- Also known as
- BNAH2 · breasts and/or nipples, aplasia or hypoplasia of, type 2 · isolated congenital breast hypoplasia/aplasia caused by mutation in PTPRF · PTPRF isolated congenital breast hypoplasia/aplasia
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