Mesomelic dwarfism, Reinhardt-Pfeiffer type (Q87103): Difference between revisions
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| Property / Canonical URI: https://id.who.int/icd/entity/1393171517 / rank | |||||||||||||||
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CID11:ID_1393171517 | |||||||||||||||
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dki-india-ID_1393171517 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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Latest revision as of 12:40, 15 August 2026
Mesomelic dwarfism, Reinhardt-Pfeiffer type is a genetic skeletal disorder characterised by disproportionate short stature from birth with dysplasia of the ulna and fibula.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1393171517 |
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| English | Mesomelic dwarfism, Reinhardt-Pfeiffer type |
Mesomelic dwarfism, Reinhardt-Pfeiffer type is a genetic skeletal disorder characterised by disproportionate short stature from birth with dysplasia of the ulna and fibula. |
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CID11:ID_1393171517
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dki-india-ID_1393171517
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Concluído
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13 August 2026
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