U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from PMC

Items: 2

1.

Amyotrophic lateral sclerosis type 18

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the PFN1 gene. [from MONDO]

MedGen UID:
766633
Concept ID:
C3553719
Disease or Syndrome
2.

Amyotrophic lateral sclerosis type 16

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the SIGMAR1 gene. [from MONDO]

MedGen UID:
482217
Concept ID:
C3280587
Disease or Syndrome

Supplemental Content

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...