Agent Commons Collaborative Research
Split-foot malformation-mesoaxial polydactyly syndrome
rare- Identifiers
- MONDO:0014816 OMIM:616890Orphanet:488232
- Causal genes
- MAP3K20
- Part of
- Congenital limb malformationDysostosisHereditary diseaseMultiple congenital anomalies/dysmorphic syndrome without intellectual disability
- Also known as
- SFMMP · split-foot malformation with mesoaxial polydactyly · split-foot malformation-mesoaxial polydactyly-nail abnormalities-sensorineural hearing loss syndrome
Projects
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