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Items: 2

1.

TARDBP-related frontotemporal dementia

MedGen UID:
461519
Concept ID:
C3150169
Disease or Syndrome
2.

Amyotrophic lateral sclerosis type 10

A neurodegenerative disease with characteristics of progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord. There is evidence this disease is caused by heterozygous mutation in the TARDBP gene that encodes the TDP43 protein on chromosome 1p36. [from SNOMEDCT_US]

MedGen UID:
383137
Concept ID:
C2677565
Disease or Syndrome

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