Disease association ontology term - MONDO:0020683 - acute disease
Term summary
ID
MONDO:0020683
Name
acute disease
Ontology or CV name
Disease association
Definition
Disease having a short and relatively severe course.
Parents
is_a
human disease
Annotation
Disease association
MONDO:0013111
-
acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
References:
PB_REF:0000006
Genes:
slm3 (SPAC23H4.04)
MONDO:0014744
-
acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
References:
PB_REF:0000006
Genes:
ppk3 (SPAC15A10.13)
MONDO:0008294
-
acute intermittent porphyria
References:
PB_REF:0000006
PMID:24782769
Genes:
hem3 (SPAC24B11.13)
MONDO:0018874
-
acute myeloid leukemia
References:
PB_REF:0000003
PB_REF:0000006
PMID:11463848
Genes:
ani1 (SPBC1347.02)
ell1 (SPBP23A10.14c)
erf4 (SPAC3F10.07c)
nup146 (SPAC23D3.06c)
ras1 (SPAC17H9.09c)
sgd1 (SPAC24C9.11)
trt1 (SPBC29A3.14c)
yap18 (SPBC19F8.03c)
MONDO:0013108
-
leukemia, acute lymphocytic, susceptibility to, 1
References:
PB_REF:0000006
Genes:
git5 (SPBC32H8.07)
nbs1 (SPBC6B1.09c)
nup146 (SPAC23D3.06c)
MONDO:0032716
-
leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate
References:
PB_REF:0000006
Genes:
plt1 (SPBC3B8.04c)
MONDO:0009992
-
myoglobinuria, acute recurrent, autosomal recessive
References:
PB_REF:0000006
Genes:
ned1 (SPAC1952.13)
