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| Term | acromesomelic dysplasia | ID (Ontology) | DOID:0080049 (Human Disease) |
| Definition | An osteochondrodysplasia that is characterized by mesomelia and acromelia, which results_in short limb dwarfism. | ||
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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 |__acromesomelic dysplasia 8 rec. |__acromesomelic dysplasia 3 1 rec. |__acromesomelic dysplasia 4 2 rec. |__acromesomelic dysplasia, Grebe type |__acromesomelic dysplasia, Hunter-Thompson type |__acromesomelic dysplasia, Maroteaux type 5 rec. |__fibular hypoplasia and complex brachydactyly |
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| Is a | osteochondrodysplasia | ||
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External Crossreferences & Linkouts
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GARD:6 MESH:C535658 ORDO:93437 |
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