Phenotypes for disease #00110 (NBIA4 (neurodegeneration, with brain iron accumulation, type 4 (NBIA-4)), OMIM:614298)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000121673 Motor neuron disease Familial 75y - - - - - - Marc Cruts 00149255
0000121742 Motor neuron disease; Corticobasal Syndrome Familial, autosomal dominant 60y - - - - - - Marc Cruts 00149326
0000121899 Motor neuron disease Familial, autosomal dominant 66y10m - - - - - - Marc Cruts 00149484
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