Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia (LAMM)

Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia(来自ICD-11)

别称:

Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia

Deafness, Congenital with Inner Ear Agenesis, Microtia, and Microdontia

Deafness with Lamm

Lamm Syndrome

Deafness, Congenital, with Labyrinthine Aplasia, Microtia, and Microdontia

Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia

Congenital Deafness with Inner Ear Agenesis, Microtia and Microdontia

Deafness, Congenital, Inner Ear Agenesis, Microtia, and Microdontia

Congenital Deafness with Inner Ear Agenesis, Microtia, Microdontia

Deafness with Labyrinthine Aplasia, Microtia, and Microdontia

Deafness with Labyrinthine Aplasia, Microtia and Microdontia

Lamm

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia, also known as congenital deafness with labyrinthine aplasia, microtia, and microdontia, is related to deafness with labyrinthine aplasia, microtia, and microdontia and skin tag. An important gene associated with Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia is FGF3 (Fibroblast Growth Factor 3). Affiliated tissues include skin and prostate, and related phenotypes are widely spaced teeth and microdontia

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