Phenotypes for disease #00759 (NBIA-2A (neurodegeneration, with brain iron accumulation, type 2A (NBIA-2A, infantile neuroaxonal dystrophy, type 1)), OMIM:256600)

6 entries on 1 page. Showing entries 1 - 6.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000060381 Infantile neuroaxonal dystrophy 1 (OMIM:256600) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080812
0000060382 Infantile neuroaxonal dystrophy 1 (OMIM:256600) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080813
0000060383 Infantile neuroaxonal dystrophy 1 (OMIM:256600) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080814
0000060384 Infantile neuroaxonal dystrophy 1 (OMIM:256600) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080815
0000060385 Infantile neuroaxonal dystrophy type 1 (OMIM:256600) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080816
0000060390 Infantile neuroaxonal dystrophy 1 (OMIM:256600) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080821
Legend   How to query