Phenotypes for disease #03238 (NCFTD (neurodegeneration due to cerebral folate deficiency), OMIM:613068)

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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     
0000060656 Neurodegeneration due to cerebral folate transport deficiency (OMIM:613068) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081087
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