Entry Search - 277700 604611 - OMIM
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Search: '277700 604611 (Search in: MIM number)'
Results: 2 entries.

2:
# 277700. WERNER SYNDROME; WRN
Cytogenetic location: 8p12
Matching terms: 277700
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
8p12 Werner syndrome 277700 AR 3 RECQL2 604611
ICD+
SNOMEDCT: 51626007
ORPHA: 902
DO: 5688
Search: 277700 604611 (Search in: MIM number)
Results: 2 entries.

1:
* 604611. RECQ PROTEIN-LIKE 2; RECQL2
Cytogenetic location: 8p12, Genomic coordinates (GRCh38): 8:31,033,810-31,176,138
Matching terms: 604611

2:
# 277700. WERNER SYNDROME; WRN
Cytogenetic location: 8p12
Matching terms: 277700