| 词条 | Johnson–McMillin syndrome |
| 释义 |
| synonyms = Alopecia-anosmia-deafness-hypogonadism syndrome | name = Johnson–McMillin syndrome | image = Autosomal dominant - en.svg | image_size = 150px | caption = Johnson–McMillin syndrome is inherited in an autosomal dominant manner | pronounce = | field = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }}Johnson–McMillin syndrome is a neuroectodermal syndrome that consist of conductive hearing loss and microtia.[1] See also
References1. ^{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |pages=831 |isbn=1-4160-2999-0 |oclc= |doi= }} External links{{Medical resources| DiseasesDB = | ICD10 = Q87.8 | ICD9 = | ICDO = | OMIM = 147770 | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = C535882 | Orphanet = 2316 }}{{DEFAULTSORT:Johnson-McMillin syndrome}} 4 : Genodermatoses|Genetic disorders with OMIM but no gene|Syndromes affecting hearing|Genetic syndromes |
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