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| Term | fibular hypoplasia and complex brachydactyly | ID (Ontology) | DOID:0050790 (Human Disease) |
| Definition | An acromesomelic dysplasia that is characterized by severe reduction or absence of the fibula and complex brachydactyly. | ||
| Also Known As | "acromesomelic dysplasia-2B" ; "Du Pan syndrome" | ||
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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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autosomal genetic disease |__autosomal recessive disease__ osteochondrodysplasia | |__acromesomelic dysplasia______| fibular hypoplasia and complex brachydactyly |
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Relationships
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| Is a |
autosomal recessive disease acromesomelic dysplasia |
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External Crossreferences & Linkouts
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KEGG:H00467 MESH:C537931 MIM:228900 ORDO:2639 |
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