| General Information | |||
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| Term | omodysplasia | ID (Ontology) | DOID:0060288 (Human Disease) |
| Definition | An osteochondrodysplasia that is characterized by severe limb shortening and facial dysmorphism. | ||
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| DO.org | |||
| Annotations | |||
| 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 |__omodysplasia 2 rec. |__omodysplasia 1 1 rec. |__omodysplasia 2 1 rec. |
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Relationships
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| Is a | osteochondrodysplasia | ||
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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MIM:PS258315 ORDO:2733 SNOMEDCT_US_2023_03_01:725164008 UMLS_CUI:C4510897 |
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