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| Term | Rapp-Hodgkin syndrome | ID (Ontology) | DOID:0060330 (Human Disease) |
| Definition | An ectodermal dysplasia characterized by abnormal development of ectodermal tissues including the skin, hair, nails, teeth and sweat glands and anhidrotic ectodermal dysplasia with cleft lip/palate. | ||
| Also Known As | "anhidrotic ectodermal dysplasia with cleft lip/palate" ; "ectodermal dysplasia syndrome, Rapp-Hodgkin type" ; "ectodermal dysplasia, Rapp-Hodgkin type" (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 dominant disease__ syndrome | |__ectodermal dysplasia________| Rapp-Hodgkin syndrome 1 rec. |
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| Is a |
autosomal dominant disease ectodermal dysplasia |
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External Crossreferences & Linkouts
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GARD:5690 MESH:C535289 MIM:129400 ORDO:3022 |
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