Phenotypes for disease #01745 (DFNB1A (deafness, autosomal recessive, type 1A (DFNB-1A, incl. di-genic)), OMIM:220290)

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000020232 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00024131
0000034029 digenic inheritance; severe deafness - - Complex - - - - - Johan den Dunnen 00043755
0000034291 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00046611
0000046748 Congenital, profound NSHL - - Familial, autosomal recessive - - - - - Zippi Brownstein 00060259
0000070575 moderate stable sensorineural hearing loss - - Familial, autosomal recessive - - - - - Johan den Dunnen 00092242
0000319554 HP:0011476 hearing loss DFNB1A Familial, autosomal recessive 02y 02y 01y HP:0011476 - Johan den Dunnen 00428306
0000319623 - Non-syndromic hearing impairment DFNB1A Familial, autosomal recessive - - - HP:0000407 - Yacouba Dia 00428724
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