Phenotypes for disease #02339 (CMT1C (Charcot-Marie-Tooth disease, type IC (CMT-1C)), OMIM:601098)

9 entries on 1 page. Showing entries 1 - 9.
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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     
0000124234 - Charcot-Marie-Tooth disease? CMT-1C Familial, autosomal dominant - - - - - Johan den Dunnen 00151871
0000124235 - Charcot-Marie-Tooth disease CMT-1C Familial, autosomal dominant - - - - - Johan den Dunnen 00151872
0000124236 - Charcot-Marie-Tooth disease CMT-1C Familial, autosomal dominant - - - - - Johan den Dunnen 00151873
0000124237 - Charcot-Marie-Tooth disease CMT-1C Familial, autosomal dominant - - - - - Johan den Dunnen 00151874
0000124238 - Charcot-Marie-Tooth disease CMT-1C Familial, autosomal dominant - - - - - Johan den Dunnen 00151875
0000124239 - Charcot-Marie-Tooth disease CMT-1C Familial, autosomal dominant - - - - - Johan den Dunnen 00151876
0000124240 - Charcot-Marie-Tooth disease CMT-1C Familial, autosomal dominant - - - - - Johan den Dunnen 00151877
0000124241 - Charcot-Marie-Tooth disease CMT-1C Familial, autosomal dominant - - - - - Johan den Dunnen 00151878
0000124242 - Charcot-Marie-Tooth disease CMT-1C Familial, autosomal dominant - - - - - Johan den Dunnen 00151879
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