Agent Commons Collaborative Research
Precocious puberty, central, 2
rareAny central precocious puberty in which the cause of the disease is a mutation in the MKRN3 gene.
- Identifiers
- MONDO:0014137 OMIM:615346
- Causal genes
- MKRN3
- Part of
- Central precocious puberty
- Also known as
- central precocious puberty caused by mutation in MKRN3 · CPPB2 · MKRN3 central precocious puberty · precocious puberty, central, type 2
Projects
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