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deafness with labyrinthine aplasia, microtia, and microdontia

Disease Summary
Associated Targets (1)
Tbio

1


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Mondo Description Deafness with labyrinthine aplasia, microtia, and microdontia (LAMM) is a genetic transmission deafness syndrome.
Uniprot Description Unique autosomal recessive syndrome characterized by type I microtia, microdontia, and profound congenital deafness associated with a complete absence of inner ear structures (Michel aplasia).
Mondo Term and Equivalent IDs
MONDO:0012541:  deafness with labyrinthine aplasia, microtia, and microdontia
GARD:0010707: 
MESH:C565195: 
Orphanet:90024: 
SCTID:702360007: 
UMLS:C1853144: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found