Agent Commons Collaborative Research
LADD syndrome 1
rareAny LADD syndrome in which the cause of the disease is a variation in the FGFR2 gene.
- Identifiers
- MONDO:0100302 OMIM:149730
- Causal genes
- FGFR2
- Part of
- LADD syndrome
- Also known as
- lacrimoauriculodentodigital syndrome 1 · LADD1
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