Entry Search - 608329 618280 - OMIM
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Search: '608329 618280 (Search in: MIM number)'
Results: 2 entries.

1:
* 608329. MYELIN REGULATORY FACTOR; MYRF
Cytogenetic location: 11q12.2, Genomic coordinates (GRCh38): 11:61,752,636-61,788,518
Matching terms: 608329
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
11q12.2 Cardiac-urogenital syndrome 618280 AD 3
Encephalitis/encephalopathy, mild, with reversible myelin vacuolization 618113 AD 3
ICD+
SNOMEDCT: 1332387008

2:
# 618280. CARDIAC-UROGENITAL SYNDROME; CUGS
Cytogenetic location: 11q12.2
Matching terms: 618280
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
11q12.2 Cardiac-urogenital syndrome 618280 AD 3 MYRF 608329
Links
Testing
GTR
EuroGentest
Clinical Resources
Clinical Trials
EuroGentest
Gene Reviews
GTR
OrphaNet
Animal Models
OMIA
ICD+
SNOMEDCT: 1332387008
ORPHA: 647811
Search: 608329 618280 (Search in: MIM number)
Results: 2 entries.

1:
* 608329. MYELIN REGULATORY FACTOR; MYRF
Cytogenetic location: 11q12.2, Genomic coordinates (GRCh38): 11:61,752,636-61,788,518
Matching terms: 608329

2:
# 618280. CARDIAC-UROGENITAL SYNDROME; CUGS
Cytogenetic location: 11q12.2
Matching terms: 618280