Disease association ontology term - MONDO:0000009 - inherited bleeding disorder, platelet-type
Term summary
ID
MONDO:0000009
Name
inherited bleeding disorder, platelet-type
Ontology or CV name
Disease association
Parents
is_a
hemorrhagic disease
is_a
blood platelet disease
is_a
hereditary disease
Annotation
Disease association
MONDO:0957580
-
bleeding disorder, platelet-type, 25
References:
PB_REF:0000006
Genes:
cdc8 (SPAC27F1.02c)
MONDO:0018794
-
cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
References:
PB_REF:0000006
Genes:
plb1 (SPAC1A6.04c)
plb2 (SPAC1786.02)
plb3 (SPAC1A6.03c)
plb4 (SPAC977.09c)
plb5 (SPCC1450.09c)
SPBC1348.10c
MONDO:0015912
-
macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
References:
PB_REF:0000006
Genes:
myo2 (SPCC645.05c)
myp2 (SPAC4A8.05c)
MONDO:0060583
-
platelet abnormalities with eosinophilia and immune-mediated inflammatory disease
References:
PB_REF:0000006
Genes:
arc1 (SPBC14C8.06)
MONDO:0014078
-
platelet-type bleeding disorder 15
References:
PB_REF:0000006
Genes:
ain1 (SPAC15A10.08)
MONDO:0014518
-
platelet-type bleeding disorder 19
References:
PB_REF:0000006
Genes:
pka1 (SPBC106.10)
