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| General Information | |||
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| Term | Weissenbacher-Zweymuller syndrome | ID (Ontology) | DOID:4258 (Human Disease) |
| Definition | An osteochondrodysplasia that results_in shortened long bones and distinct facial abnormalities. | ||
| Also Known As | "Piere-Robin syndrome" ; "Pierre Robin Malformation" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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bone development disease__ cartilage disease_________| osteochondrodysplasia |__Weissenbacher-Zweymuller syndrome |
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| Is a | osteochondrodysplasia | ||
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External Crossreferences & Linkouts
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ICD10CM:Q87.0 MESH:D010855 MIM:261800 NCI:C85010 SNOMEDCT_US_2023_03_01:156908005 UMLS_CUI:C0031900 |
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