Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Term ID:3073
Name:Deafness, autosomal recessive 51
Definition:
Alternative IDs:OMIM:609941
ParentIDs:MESH:D006313
TreeNumbers:C09.218.458.341.887.432/C538202 |C09.218.807.186.432/C538202 |C10.228.140.068.432/C538202 |C10.597.751.418.341.887.432/C538202 |C23.888.592.763.393.341.887.432/C538202
Synonyms:DFNB51
Slim Mappings:Ear-nose-throat disease|Nervous system disease|Signs and symptoms
Reference: MedGen: C538202
MeSH: C538202
OMIM: 609941;

Genes: DFNB51;
Phenotypes
1 HP:0000007Autosomal recessive inheritance
2 HP:0000407Sensorineural hearing impairment
Disease Causing ClinVar Variants