Disease association ontology term - MONDO:0005144 - familial amyotrophic lateral sclerosis
Term summary
ID
MONDO:0005144
Name
familial amyotrophic lateral sclerosis
Ontology or CV name
Disease association
Definition
An instance of amyotrophic lateral sclerosis that is caused by an inherited modification of the individual's genome.
Parents
is_a
amyotrophic lateral sclerosis
is_a
hereditary motor neuron disease
Annotation
Disease association
MONDO:0859529
-
amyotrophic lateral sclerosis 27, juvenile
References:
PB_REF:0000006
Genes:
lcb1 (SPBC18E5.02c)
MONDO:0007103
-
amyotrophic lateral sclerosis type 1
References:
PB_REF:0000006
Genes:
sod1 (SPAC821.10c)
tip1 (SPAC3C7.12)
MONDO:0012945
-
amyotrophic lateral sclerosis type 11
References:
PB_REF:0000006
Genes:
fig4 (SPAC1093.03)
MONDO:0010459
-
amyotrophic lateral sclerosis type 15
References:
PB_REF:0000006
Genes:
dsk2 (SPAC26A3.16)
MONDO:0013715
-
amyotrophic lateral sclerosis type 16
References:
PB_REF:0000006
Genes:
erg2 (SPAC20G8.07c)
MONDO:0014531
-
amyotrophic lateral sclerosis type 22
References:
PB_REF:0000006
Genes:
atb2 (SPBC800.05c)
nda2 (SPBC16A3.15c)
MONDO:0011223
-
amyotrophic lateral sclerosis type 4
References:
PB_REF:0000006
Genes:
dbl8 (SPBC29A10.10c)
sen1 (SPAC6G9.10c)
MONDO:0012077
-
amyotrophic lateral sclerosis type 8
References:
PB_REF:0000006
PMID:15372378
Genes:
scs2 (SPBC16G5.05c)
scs22 (SPAC17C9.12)
MONDO:0014395
-
frontotemporal dementia and/or amyotrophic lateral sclerosis 2
References:
PB_REF:0000006
Genes:
mix17 (SPAC6C3.02c)
MONDO:0013501
-
frontotemporal dementia and/or amyotrophic lateral sclerosis 6
References:
PB_REF:0000006
Genes:
cdc48 (SPAC1565.08)
MONDO:0010936
-
frontotemporal dementia and/or amyotrophic lateral sclerosis 7
References:
PB_REF:0000006
Genes:
did4 (SPAC4F8.01)
MONDO:0008458
-
spinocerebellar ataxia type 2
References:
PB_REF:0000006
Genes:
ath1 (SPBC21B10.03c)
