Amyotrophic Lateral Sclerosis 22 with or Without Frontotemporal Dementia (ALS22)

Alias:

Als22

Sclerosis, Lateral, Amyotrophic, Type 22 with/without Frontotemoral Dementia

Amyotrophic Lateral Sclerosis 22, with or Without Frontotemporal Dementia

Amyotrophic Lateral Sclerosis Type 22

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Amyotrophic Lateral Sclerosis 22 with or Without Frontotemporal Dementia, also known as als22, is related to amyotrophic lateral sclerosis type 22. An important gene associated with Amyotrophic Lateral Sclerosis 22 with or Without Frontotemporal Dementia is TUBA4A (Tubulin Alpha 4a). Affiliated tissues include spinal cord and brain, and related phenotypes are amyotrophic lateral sclerosis and frontotemporal dementia

Related ID：

MALACARDS：AMY099

OMIM：616208

MESH：D000690