Phenotypes for disease #02254 (CMTX5 (Charcot-Marie-Tooth disease, X-linked recessive, type 5 (CMTX-5)), OMIM:311070)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000155122 sensori-motor neuropathy since the age of 8 profound bilateral hearing loss bilateral optic neuropathy - - Familial, X-linked 35y 35y 08y 15y - Justine Lerat 00207340
0000204016 hearing loss, epilepsy, peripheral neuropathy, severe IUGR - - Isolated (sporadic) - 00y06m - - - Laurence Jonard 00266240
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