Phenotypes for disease #02709 (CMT2K (Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K), OMIM:607831)

5 entries on 1 page. Showing entries 1 - 5.
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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     
0000081601 Charcot-Marie-Tooth disease 2K, axonal - - Unknown - - - - - Johan den Dunnen 00103670
0000081627 Charcot-Marie-Tooth disease 2K, axonal - - Unknown - - - - - Johan den Dunnen 00103696
0000081631 Charcot-Marie-Tooth disease 2K - - Unknown - - - - - Johan den Dunnen 00103700
0000081645 Charcot-Marie-Tooth disease 2K, axonal - - Unknown - - - - - Johan den Dunnen 00103714
0000291711 see paper; ..., peripheral neuropathy (HP:0009830), No decreased nerve conduction velocity (-HP:0000762) CMT CMT2K Familial, autosomal dominant 69y - 57y Peripheral neuropathy (HP:0009830), No decreased nerve conduction velocity (-HP:0000762) - Yvet den Hartog 00398625
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