Acrofacial dysostosis, Weyers type (Q86225): Difference between revisions
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Revision as of 11:35, 15 August 2026
Acrofacial dysostosis, Weyers type is a type of acrofacial dysostoses, a heterogenous group of disorders combining defects of limbs and mandibular/facial development. Acrofacial dysostosis Weyers type is a rare autosomal dominant condition of mild phenotype. Dental anomalies, nail dystrophy, postaxial polydactyly, and mild short stature are associated to a normal intelligence.
| Language | Label | Description | Also known as |
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| default for all languages | ID_547338814 |
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| English | Acrofacial dysostosis, Weyers type |
Acrofacial dysostosis, Weyers type is a type of acrofacial dysostoses, a heterogenous group of disorders combining defects of limbs and mandibular/facial development. Acrofacial dysostosis Weyers type is a rare autosomal dominant condition of mild phenotype. Dental anomalies, nail dystrophy, postaxial polydactyly, and mild short stature are associated to a normal intelligence. |
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CID11:ID_547338814
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dki-india-ID_547338814
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Concluído
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