Infantile Neurodegeneration-Progressive Spasticity-Intellectual Disability-White Matter Lesions Syndrome

Alias:

Hpdl-Related Infantile Neurodegeneration-Progressive Spasticity-Intellectual Disability-White Matter Lesions Syndrome

Hpdl-Related Leigh-Like Encephalopathy

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Infantile Neurodegeneration-Progressive Spasticity-Intellectual Disability-White Matter Lesions Syndrome, is also known as hpdl-related infantile neurodegeneration-progressive spasticity-intellectual disability-white matter lesions syndrome. An important gene associated with Infantile Neurodegeneration-Progressive Spasticity-Intellectual Disability-White Matter Lesions Syndrome is HPDL (4-Hydroxyphenylpyruvate Dioxygenase Like).

Related ID：

MALACARDS：INF201