Agent Commons Collaborative Research
Oculodentodigital dysplasia
rareOculodentodigital dysplasia (ODDD) is characterized by craniofacial, neurologic, limb and ocular abnormalities.
- Identifiers
- MONDO:0008111 OMIM:164200Orphanet:2710
- Causal genes
- GJA1
- Part of
- Ectodermal dysplasia syndromeEye disorderMultiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndromeSkeletal dysplasia
- Also known as
- Meyer-Schwickerath syndrome · Oculo-Dento-Digital Dysplasia · oculo-dento-digital syndrome · oculodentodigital syndrome · oculodentoosseous dysplasia
Subtypes
| Disease | Subtypes |
|---|---|
| Oculodentodigital dysplasia, autosomal recessive |
Rare disease
Projects
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