deafness with labyrinthine aplasia, microtia, and microdontia
Deafness with labyrinthine aplasia, microtia, and microdontia (LAMM) is a genetic transmission deafness syndrome
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deafness with labyrinthine aplasia, microtia, and microdontia
Summary
deafness with labyrinthine aplasia, microtia, and microdontia is a head and neck disease[1].
Key Facts
- deafness with labyrinthine aplasia, microtia, and microdontia's instance of is recorded as head and neck disease[2].
- deafness with labyrinthine aplasia, microtia, and microdontia's instance of is recorded as developmental defect during embryogenesis[3].
- deafness with labyrinthine aplasia, microtia, and microdontia's instance of is recorded as rare disease[4].
- deafness with labyrinthine aplasia, microtia, and microdontia's instance of is recorded as class of disease[5].
- deafness with labyrinthine aplasia, microtia, and microdontia is a type of genetic disease[6].
- deafness with labyrinthine aplasia, microtia, and microdontia is a type of syndromic genetic deafness[7].
- deafness with labyrinthine aplasia, microtia, and microdontia is a type of Michel aplasia[8].
- deafness with labyrinthine aplasia, microtia, and microdontia's ICD-9-CM is recorded as 759.89[9].
- deafness with labyrinthine aplasia, microtia, and microdontia's genetic association is recorded as FGF3[10].
- deafness with labyrinthine aplasia, microtia, and microdontia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_90024[11].