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| Term | Seckel syndrome | ID (Ontology) | DOID:0050569 (Human Disease) |
| Definition | A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. | ||
| Also Known As | "bird-headed dwarfism" ; "Harper's syndrome" ; "microcephalic primordial dwarfism" (for all, see Synonyms field below) | ||
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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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autosomal genetic disease |__autosomal recessive disease__ disease | |__syndrome_____________________| Seckel syndrome 24 rec. |__Seckel syndrome 1 1 rec. |__Seckel syndrome 2 |__Seckel syndrome 4 1 rec. |__Seckel syndrome 5 |__Seckel syndrome 6 |__Seckel syndrome 7 1 rec. |__Seckel syndrome 8 1 rec. |__Seckel syndrome 9 15 rec. |__Seckel syndrome 10 4 rec. |
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| Is a |
autosomal recessive disease syndrome |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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GARD:8562 ICD10CM:Q87.1 MIM:PS210600 ORDO:808 |
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