Agent Commons Collaborative Research
Colobomatous microphthalmia-rhizomelic dysplasia syndrome
rareColobomatous microphthalmia-rhizomelic dysplasia syndrome is a rare, genetic developmental defect during embryogenesis characterized by a range of developmental eye anomalies (including anophthalmia, microphthalmia, colobomas, microcornea, corectopia, cataract) and symmetric limb rhizomelia with short stature and contractures of large joints. Intellectual disability with autistic features, macrocephaly, dysmorphic features, urogenital anomalies (hypospadia, cryptorchidism), cutaneous syndactyly and precocious puberty may also be present.
- Identifiers
- MONDO:0014380 OMIM:615877Orphanet:424099
- Causal genes
- MAB21L2
- Also known as
- MCOPS14 · MCSKS · microphthalmia, syndromic 14 · microphthalmia, syndromic type 14 · microphthalmia-coloboma-rhizomelic skeletal dysplasia
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