Cranioectodermal dysplasia (Q83095)
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Cranioectodermal dysplasia (CED) is a rare developmental disorder characterised by congenital skeletal and ectodermal defects associated with dysmorphic features, nephronophthisis, hepatic fibrosis and ocular anomalies (mainly retinitis pigmentosa).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1588881145 |
||
| English | Cranioectodermal dysplasia |
Cranioectodermal dysplasia (CED) is a rare developmental disorder characterised by congenital skeletal and ectodermal defects associated with dysmorphic features, nephronophthisis, hepatic fibrosis and ocular anomalies (mainly retinitis pigmentosa). |
Statements
CID11:ID_1588881145
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dki-india-ID_1588881145
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Concluído
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13 August 2026
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