Phenotypes for disease #01011 (DFNA20;DFNA26 (deafness, autosomal dominant, type 20/26 (DFNA-20;DFNA-26)), OMIM:604717)

5 entries on 1 page. Showing entries 1 - 5.
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Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000220905 severe to profound bilateral deafness and cleft lip and palate Hearing loss Hearing loss Familial, autosomal dominant 04y06m - 00y - - Camille Cenni 00287170
0000221097 moderate hearing loss downward slope into higher frequencies with a gradual worsening over time affecting all frequencies NSHL NSHL Familial, autosomal dominant 29y 15y 15y - - Camille Cenni 00287173
0000221996 bilateral, symmetrical and progressive sensorineural hearing loss at mid- and high frequencies (a down-sloping audiometric profile) of post-lingual onset (third decade) Deafness Deafness Familial, autosomal dominant - - - HP:0000407 - Camille Cenni 00288259
0000221997 post-lingual, bilateral, symmetrical and progressive sensorineural hearing impairment that affect the mid- and high frequencies. hearing problems at school age. Deafness Deafness Familial, autosomal dominant - - - HP:0000407 - Camille Cenni 00288260
0000222983 Before they were 15 years old, the patients had already shown gently downsloping audiograms. By ages 15 to 20 and 25 to 40 years, hearing loss had become severe to profound at 8 kHz and 1 to 4 kHz, respectively. The thresholds at 0.25 to 0.5 kHz showed more gradual progression at an average increase of about 1.5 to 2 dB/y. Deafness Deafness Familial, autosomal dominant - - - - - Camille Cenni 00289370
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