Entry Search - 235200 613609 - OMIM
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Search: '235200 613609 (Search in: MIM number)'
Results: 2 entries.

1:
* 613609. HOMEOSTATIC IRON REGULATOR; HFE
Cytogenetic location: 6p22.2, Genomic coordinates (GRCh38): 6:26,087,429-26,098,343
Matching terms: 613609
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
6p22.2 Hemochromatosis, type 1 235200 AR 3
ICD+
SNOMEDCT: 1186847009

2:
# 235200. HEMOCHROMATOSIS, TYPE 1; HFE1
Cytogenetic locations: 6p22.2, 20p12.3
Matching terms: 235200
 Phenotype-Gene Relationships   Phenotypic Series   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
6p22.2 Hemochromatosis, type 1 235200 AR 3 HFE 613609
20p12.3 {HFE hemochromatosis, modifier of} 235200 AR 3 BMP2 112261
ICD+
SNOMEDCT: 1186847009, 35400008, 399053004, 399170009
ICD10CM: E83.110
ICD9CM: 275.01
ORPHA: 465508
DO: 0111029
Search: 235200 613609 (Search in: MIM number)
Results: 2 entries.

1:
* 613609. HOMEOSTATIC IRON REGULATOR; HFE
Cytogenetic location: 6p22.2, Genomic coordinates (GRCh38): 6:26,087,429-26,098,343
Matching terms: 613609

2:
# 235200. HEMOCHROMATOSIS, TYPE 1; HFE1
Cytogenetic locations: 6p22.2, 20p12.3
Matching terms: 235200