Entry Search - 190020 218040 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '190020 218040 (Search in: MIM number)'
Results: 2 entries.

1:
* 190020. HRAS PROTOONCOGENE, GTPase; HRAS
Cytogenetic location: 11p15.5, Genomic coordinates (GRCh38): 11:532,242-535,576
Matching terms: 190020
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
11p15.5 Bladder cancer, somatic 109800 3
Congenital myopathy with excess of muscle spindles 218040 AD 3
Costello syndrome 218040 AD 3
Nevus sebaceous or woolly hair nevus, somatic 162900 3
Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic 163200 3
Spitz nevus or nevus spilus, somatic 137550 3
Thyroid carcinoma, follicular, somatic 188470 3
ICD+
SNOMEDCT: 309776008

2:
# 218040. COSTELLO SYNDROME; CSTLO
MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES, INCLUDED; CMEMS, INCLUDED
Cytogenetic locations: 11p15.5,
Matching terms: 218040
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
11p15.5 Costello syndrome 218040 AD 3 HRAS 190020
11p15.5 Congenital myopathy with excess of muscle spindles 218040 AD 3 HRAS 190020
ICD+
SNOMEDCT: 309776008
ORPHA: 3071
DO: 0050469
Search: 190020 218040 (Search in: MIM number)
Results: 2 entries.

1:
* 190020. HRAS PROTOONCOGENE, GTPase; HRAS
Cytogenetic location: 11p15.5, Genomic coordinates (GRCh38): 11:532,242-535,576
Matching terms: 190020

2:
# 218040. COSTELLO SYNDROME; CSTLO
MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES, INCLUDED; CMEMS, INCLUDED
Cytogenetic locations: 11p15.5,
Matching terms: 218040