Phenotypes for disease #02357 (DFNB12 (deafness, autosomal recessive, type 12 (DFNB-12)), OMIM:601386)

6 entries on 1 page. Showing entries 1 - 6.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000045610 congenital severe hearing loss - - Familial, autosomal recessive - - - - - Mary-Claire King 00059022
0000046726 Congenital, profound NSHL - - Familial, autosomal recessive - - - - - Zippi Brownstein 00060241
0000046727 Congenital profound NSHL - - Familial, autosomal recessive - - - - - Zippi Brownstein 00060242
0000060653 Deafness, autosomal recessive 12 (OMIM:601386) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081084
0000238715 - Hearing loss - Familial, autosomal recessive 18y - - - - Khushnooda Ramzan 00314956
0000351726 Myopathy Axial muscle weakness Muscle weakness Proximal muscle weakness Joint hypermobility Congenital sensorineural hearing impairment Congenital myopathy - Unknown - - - - - Camille Verebi 00466362
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