| 词条 | Genodermatosis |
| 释义 |
| name = Genodermatosis | synonyms = | image = | caption = | pronounce = | field = dermatology | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }} Genodermatoses are inherited genetic skin conditions often grouped into three categories: chromosomal, single gene, and polygenetic.[1]{{rp|547}} Types
See also
References1. ^James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. {{ISBN|0-7216-2921-0}}. External links{{Medical resources| DiseasesDB = | ICD10 = | ICD9 = | ICDO = | OMIM = | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = D012873 }}{{Congenital malformations and deformations of integument}}{{genetic-disorder-stub}}{{genodermatoses-stub}} 1 : Genodermatoses |
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