Phenotypes for disease #02338 (DFNB9;AUNB1 (deafness, autosomal recessive, type 9), OMIM:601071)

13 entries on 1 page. Showing entries 1 - 13.
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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     
0000045641 congenital, profound HL, auditory neuropathy - - Familial, autosomal recessive - - - - - Zippi Brownstein 00059051
0000188533 auditory neuropathy - - Familial - - - - - Sophie Achard 00249660
0000188534 auditory neuropathy - - Familial, autosomal recessive - - - - - Sophie Achard 00249661
0000188535 Auditory neuropathy profound deafness - - Familial, autosomal recessive - - - - - Sophie Achard 00249662
0000188592 auditory neuropathy - - Isolated (sporadic) - - - - - Sophie Achard 00249723
0000230584 auditory neuropathy - - Familial, autosomal recessive - - 01y - - Sophie Achard 00303507
0000230586 HP:0008504Moderate sensorineural hearing impairment temperature sensitive auditory neuropathy - - Isolated (sporadic) - - - - - Sophie Achard 00303509
0000230587 HP:0008527Congenital sensorineural hearing impairment profound deafness auditory neuropathy - - Isolated (sporadic) - 00y05m 00y05m - - Sophie Achard 00303510
0000230590 HP:0008527 Congenital sensorineural hearing impairment Profound deafness auditory neuropathy - - Isolated (sporadic) - - - - - Sophie Achard 00303513
0000230591 HP:0008527Congenital sensorineural hearing impairment Auditory neuropathy - - Unknown - - - - - Sophie Achard 00303514
0000230592 HP:0008527Congenital sensorineural hearing impairment Auditory neuropathy - - Isolated (sporadic) - 01y 01y 01y - Sophie Achard 00303515
0000319321 - Non-syndromic hearing impairment Non-syndromic hearing impairment Familial, autosomal recessive - - - HP:0000399 - Yacouba Dia 00428415
0000337685 - Severe Hearing Loss - Unknown - - - - - Hina Khan 00448502
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