Disease association ontology term - MONDO:0020297 - Noonan syndrome and Noonan-related syndrome
Term summary
ID
MONDO:0020297
Name
Noonan syndrome and Noonan-related syndrome
Ontology or CV name
Disease association
Parents
is_a
RASopathy
is_a
disorder of development or morphogenesis
is_a
familial hypertrophic cardiomyopathy
Annotation
Disease association
MONDO:0015280
-
cardiofaciocutaneous syndrome
References:
PB_REF:0000006
Genes:
byr1 (SPAC1D4.13)
pek1 (SPBC543.07)
ras1 (SPAC17H9.09c)
wis1 (SPBC409.07c)
MONDO:0007265
-
cardiofaciocutaneous syndrome 1
References:
PB_REF:0000003
Genes:
ras1 (SPAC17H9.09c)
MONDO:0014112
-
cardiofaciocutaneous syndrome 2
References:
PB_REF:0000006
Genes:
ras1 (SPAC17H9.09c)
MONDO:0014113
-
cardiofaciocutaneous syndrome 3
References:
PB_REF:0000006
Genes:
byr1 (SPAC1D4.13)
pek1 (SPBC543.07)
wis1 (SPBC409.07c)
MONDO:0014114
-
cardiofaciocutaneous syndrome 4
References:
PB_REF:0000006
Genes:
byr1 (SPAC1D4.13)
pek1 (SPBC543.07)
wis1 (SPBC409.07c)
MONDO:0009026
-
Costello syndrome
References:
PB_REF:0000006
Genes:
ras1 (SPAC17H9.09c)
MONDO:0018997
-
Noonan syndrome
References:
PB_REF:0000006
Genes:
ras1 (SPAC17H9.09c)
MONDO:0033669
-
Noonan syndrome 13
References:
PB_REF:0000006
Genes:
spk1 (SPAC31G5.09c)
MONDO:0012371
-
Noonan syndrome 3
References:
PB_REF:0000006
Genes:
ras1 (SPAC17H9.09c)
MONDO:0013186
-
Noonan syndrome 6
References:
PB_REF:0000006
Genes:
ras1 (SPAC17H9.09c)
MONDO:0054588
-
Noonan syndrome-like disorder with loose anagen hair 2
References:
PB_REF:0000006
Genes:
dis2 (SPBC776.02c)
sds21 (SPCC31H12.05c)