Phenotypes for disease #00759 (NBIA2A (neurodegeneration, with brain iron accumulation, type 2A (NBIA-2A, infantile neuroaxonal dystrophy, type 1)), OMIM:256600)

7 entries on 1 page. Showing entries 1 - 7.
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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     
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
0000274642 DD; ID; seizures; cerebellar atrophy (Neurological) - Infantile neuroaxonal dystrophy 1 Familial - - - - - LOVD 00380789
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