Disease association ontology term - MONDO:0700007 - idiopathic disease
Term summary
ID
MONDO:0700007
Name
idiopathic disease
Ontology or CV name
Disease association
Definition
A disease or disorder for which the cause is of uncertain or unknown.
Parents
is_a
disease by etiologic mechanism
Annotation
Disease association
MONDO:0014628
-
basal ganglia calcification, idiopathic, 6
References:
PB_REF:0000006
Genes:
spx2 (SPCC1827.07c)
MONDO:0019006
-
familial idiopathic steroid-resistant nephrotic syndrome
References:
PB_REF:0000003
Genes:
nup37 (SPAC4F10.18)
nup85 (SPBC17G9.04c)
rga5 (SPBC17F3.01c)
MONDO:0013836
-
familial steroid-resistant nephrotic syndrome with sensorineural deafness
References:
PB_REF:0000006
Genes:
coq6 (SPBC146.12)
MONDO:0011303
-
focal segmental glomerulosclerosis 1
References:
PB_REF:0000006
Genes:
ain1 (SPAC15A10.08)
MONDO:0015713
-
idiopathic central precocious puberty
References:
PB_REF:0000003
Genes:
cps3 (SPAC3A11.02)
MONDO:0014752
-
nephrotic syndrome, type 11
References:
PB_REF:0000006
Genes:
nup107 (SPBC428.01c)
MONDO:0014817
-
nephrotic syndrome, type 12
References:
PB_REF:0000006
Genes:
npp106 (SPCC1739.14)
nup97 (SPCC1620.11)
MONDO:0014818
-
nephrotic syndrome, type 13
References:
PB_REF:0000006
Genes:
nup186 (SPCC290.03c)
MONDO:0014099
-
nephrotic syndrome, type 8
References:
PB_REF:0000006
Genes:
rdi1 (SPAC6F12.06)
MONDO:0014257
-
nephrotic syndrome, type 9
References:
PB_REF:0000006
Genes:
coq8 (SPBC2D10.18)
