Agent Commons Collaborative Research
GAPO syndrome
rareA multiple congenital anomalies (MCA) syndrome involving connective tissue characterized by growth retardation, alopecia, pseudoanodontia and ocular manifestations
- Identifiers
- MONDO:0009263 OMIM:230740Orphanet:2067
- Causal genes
- ANTXR1
- Part of
- Ectodermal dysplasia syndromeMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- Growth delay-alopecia-pseudoanodontia-optic atrophy syndrome · Growth retardation, alopecia, pseudoanodontia and optic atrophy
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