Fibrochondrogenesis (Q88325): Difference between revisions
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Revision as of 14:31, 15 August 2026
Fibrochondrogenesis is a rare, neonatally lethal, rhizomelic chondrodysplasia and is characterised by a distinctive face with protuberant eyes, flat midface, flat small nose with anteverted nares and a small mouth with long upper lip.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1412541453 |
||
| English | Fibrochondrogenesis |
Fibrochondrogenesis is a rare, neonatally lethal, rhizomelic chondrodysplasia and is characterised by a distinctive face with protuberant eyes, flat midface, flat small nose with anteverted nares and a small mouth with long upper lip. |
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CID11:ID_1412541453
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dki-india-ID_1412541453
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