Disease association ontology term - MONDO:0021189 - intestinal motility disease
Term summary
ID
MONDO:0021189
Name
intestinal motility disease
Ontology or CV name
Disease association
Definition
A disease that has its basis in the disruption of intestinal motility.
Parents
is_a
intestinal disorder
Annotation
Disease association
MONDO:0012730
-
aortic aneurysm, familial thoracic 6
References:
PB_REF:0000006
Genes:
act1 (SPBC32H8.12c)
MONDO:0025708
-
megacystis-microcolon-intestinal hypoperistalsis syndrome 2
References:
PB_REF:0000006
Genes:
myo2 (SPCC645.05c)
myp2 (SPAC4A8.05c)
MONDO:0030296
-
megacystis-microcolon-intestinal hypoperistalsis syndrome 4
References:
PB_REF:0000006
Genes:
rlc1 (SPAC926.03)
MONDO:0030329
-
megacystis-microcolon-intestinal hypoperistalsis syndrome 5
References:
PB_REF:0000006
Genes:
act1 (SPBC32H8.12c)
MONDO:0013542
-
Moyamoya disease 5
References:
PB_REF:0000006
Genes:
act1 (SPBC32H8.12c)
MONDO:0013452
-
multisystemic smooth muscle dysfunction syndrome
References:
PB_REF:0000006
Genes:
act1 (SPBC32H8.12c)
MONDO:0020754
-
visceral myopathy 1
References:
PB_REF:0000006
Genes:
act1 (SPBC32H8.12c)
MONDO:0859157
-
visceral myopathy 2
References:
PB_REF:0000006
Genes:
myo2 (SPCC645.05c)
myp2 (SPAC4A8.05c)