Phenotypes for disease #02557 (CMT2B2 (Charcot-Marie-Tooth disease, axonal, type 2B2), OMIM:605589)

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     
0000025704 see paper - - Familial, autosomal recessive - - - - - Johan den Dunnen 00029693
0000291860 Peripheral neuropathy (HP:0009830), no decreased nerve conduction velocity (-HP:0000762) CMT - Familial, autosomal recessive 53y - 50y Peripheral neuropathy (HP:0009830), no decreased nerve conduction velocity (-HP:0000762) - Yvet den Hartog 00398776
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