Phenotypes for disease #05363 (ANOA;MMDS9A (neuropathy, auditory, and optic atrophy), OMIM:617717)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000119736 - - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00147019
0000119737 - - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00147020
0000119738 - - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00147021
0000119739 - - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00147022
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