Weissenbacher- Zweymuller syndrome (Q88326): Difference between revisions
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dki-india-ID_1421501711 | |||||||||||||||
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13 August 2026
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Latest revision as of 14:31, 15 August 2026
Weissenbacher-Zweymuller syndrome is a genetic disorder characterised by short stature at birth, neonatal micrognathia, cleft palate, rhizomelic chondrodysplasia with 'dumbbell' shaped arm and leg bones, hypertelorism and vertebral coronal clefts.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1421501711 |
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| English | Weissenbacher- Zweymuller syndrome |
Weissenbacher-Zweymuller syndrome is a genetic disorder characterised by short stature at birth, neonatal micrognathia, cleft palate, rhizomelic chondrodysplasia with 'dumbbell' shaped arm and leg bones, hypertelorism and vertebral coronal clefts. |
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CID11:ID_1421501711
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dki-india-ID_1421501711
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Concluído
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13 August 2026
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