Hereditary hemochromatosis - OMIM - NCBI

Hereditary hemochromatosis - OMIM - NCBI



From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.

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• Search OMIM for "Hereditary hemochromatosis" 

1.

#235200 - HEMOCHROMATOSIS, TYPE 1; HFE1

Cytogenetic locations: 1pter-p36.13, 20p12.3

OMIM:

 

235200

Gene summaries Genetic tests Medical literature

Select item 6042502.

#604250 - HEMOCHROMATOSIS, TYPE 3; HFE3

Cytogenetic locations: 7q22.1

OMIM:

 

604250

Gene summaries Genetic tests Medical literature

Select item 6060693.

#606069 - HEMOCHROMATOSIS, TYPE 4; HFE4

Cytogenetic locations: 2q32.2

OMIM:

 

606069

Gene summaries Genetic tests Medical literature

Select item 6133134.

#613313 - HEMOCHROMATOSIS, TYPE 2B; HFE2B

Cytogenetic locations: 19q13.12

OMIM:

 

613313

Gene summaries Genetic tests Medical literature

Select item 6155175.

#615517 - HEMOCHROMATOSIS, TYPE 5; HFE5

Cytogenetic locations: 11q12.3

OMIM:

 

615517

Gene summaries Genetic tests Medical literature

Select item 6023906.

#602390 - HEMOCHROMATOSIS, TYPE 2A; HFE2A

HEMOCHROMATOSIS, TYPE 2, INCLUDED; HFE2, INCLUDED

Cytogenetic locations: 1q21.1

OMIM:

 

602390

Gene summaries Genetic tests Medical literature

Select item 2311007.

231100 - HEMOCHROMATOSIS, NEONATAL

OMIM:

 

231100

Gene summaries Genetic tests Medical literature

Select item 1056008.

%105600 - ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE III; CDAN3

Cytogenetic locations: 15q21

OMIM:

 

105600

Gene summaries Genetic tests Medical literature

Select item 3007519.

#300751 - ANEMIA, SIDEROBLASTIC, 1; SIDBA1

Cytogenetic locations: Xp11.21

OMIM:

 

300751

Gene summaries Genetic tests Medical literature

Select item 18290010.

#182900 - SPHEROCYTOSIS, TYPE 1; SPH1

Cytogenetic locations: 8p11.21

OMIM:

 

182900

Gene summaries Genetic tests Medical literature

Select item 22410011.

#224100 - ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE II; CDAN2

Cytogenetic locations: 20p11.23

OMIM:

 

224100

Gene summaries Genetic tests Medical literature

Select item 60837412.

*608374 - HEMOJUVELIN; HJV

Cytogenetic locations: 1q21.1

OMIM:

 

608374

Gene summaries Genetic tests Medical literature

Select item 60472013.

*604720 - TRANSFERRIN RECEPTOR 2; TFR2

Cytogenetic locations: 7q22.1

OMIM:

 

604720

Gene summaries Genetic tests Medical literature

Select item 61360914.

*613609 - HFE GENE; HFE

Cytogenetic locations: 6p22.2

OMIM:

 

613609

Gene summaries Genetic tests Medical literature

Select item 60465315.

*604653 - SOLUTE CARRIER FAMILY 40 (IRON-REGULATED TRANSPORTER), MEMBER 1; SLC40A1

Cytogenetic locations: 2q32.2

OMIM:

 

604653

Gene summaries Genetic tests Medical literature

Select item 60646416.

*606464 - HEPCIDIN ANTIMICROBIAL PEPTIDE; HAMP

Cytogenetic locations: 19q13.12

OMIM:

 

606464

Gene summaries Genetic tests Medical literature

Select item 13477017.

*134770 - FERRITIN HEAVY CHAIN 1; FTH1

Cytogenetic locations: 11q12.3

OMIM:

 

134770

Gene summaries Genetic tests Medical literature

Select item 30130018.

*301300 - DELTA-AMINOLEVULINATE SYNTHASE 2; ALAS2

Cytogenetic locations: Xp11.21

OMIM:

 

301300

Gene summaries Genetic tests Medical literature

Select item 60574519.

*605745 - CYTOCHROME b REDUCTASE 1; CYBRD1

OMIM:

 

605745

Gene summaries Genetic tests Medical literature

Select item 61104920.

*611049 - SOLUTE CARRIER FAMILY 17, MEMBER 2; SLC17A2

Cytogenetic locations: 6p22.2

OMIM:

 

611049

Gene summaries Genetic tests Medical literature