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

Alias:

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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Medical Symptom

Gene & Mutation

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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

Related ID：

MALACARDS：DFN358

OMIM：610706