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| Term | ectodermal dysplasia 13 | ID (Ontology) | DOID:0111650 (Human Disease) |
| Definition | An ectodermal dysplasia characterized by severe oligodontia accompanied by anomalies of hair and skin that has_material_basis_in homozygous or compound heterozygous mutation in the KREMEN1 gene on chromosome 22q12.1. | ||
| Also Known As | "ECTD13" ; "ectodermal dysplasia 13, hair/tooth type" | ||
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| DO.org | |||
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autosomal genetic disease |__autosomal recessive disease__ syndrome | |__ectodermal dysplasia_________| ectodermal dysplasia 13 |
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autosomal recessive disease ectodermal dysplasia |
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| MIM:617392 | |||