hemochromatosis - OMIM - NCBI

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Select item 6022541.

*602254 - SRR1 DOMAIN-CONTAINING PROTEIN; SRRD

Cytogenetic locations: #8806657

OMIM:: 602254

Gene summaries Genetic tests Medical literature

Select item 6042502.

#604250 - HEMOCHROMATOSIS, TYPE 3; HFE3

Cytogenetic locations: 12130528

OMIM:: 604250

Gene summaries Genetic tests Medical literature

Select item 6060693.

#606069 - HEMOCHROMATOSIS, TYPE 4; HFE4

Cytogenetic locations: contiguous

OMIM:: 606069

Gene summaries Genetic tests Medical literature

Select item 6133134.

#613313 - HEMOCHROMATOSIS, TYPE 2B; HFE2B

Cytogenetic locations: 10205270

OMIM:: 613313

Gene summaries Genetic tests Medical literature

Select item 6155175.

#615517 - HEMOCHROMATOSIS, TYPE 5; HFE5

Cytogenetic locations: 11389486

OMIM:: 615517

Gene summaries Genetic tests Medical literature

Select item 6023906.

#602390 - HEMOCHROMATOSIS, TYPE 2A; HFE2A

HEMOCHROMATOSIS, TYPE 2, INCLUDED; HFE2, INCLUDED

Cytogenetic locations: FAM72C

OMIM:: 602390

Gene summaries Genetic tests Medical literature

Select item 2352007.

#235200 - HEMOCHROMATOSIS, TYPE 1; HFE1

Cytogenetic locations: 1p36, 1p36

OMIM:: 235200

Gene summaries Genetic tests Medical literature

Select item 3010728.

#301072 - NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HEMOCHROMATOSIS; NEDEPH

Cytogenetic locations: 24259288

OMIM:: 301072

Gene summaries Genetic tests Medical literature

Select item 2311009.

231100 - HEMOCHROMATOSIS, NEONATAL

OMIM:: 231100

Gene summaries Genetic tests Medical literature

Select item 60837410.

*608374 - HEMOJUVELIN BMP CORECEPTOR; HJV

Cytogenetic locations: FAM72C

OMIM:: 608374

Gene summaries Genetic tests Medical literature

Select item 60472011.

*604720 - TRANSFERRIN RECEPTOR 2; TFR2

Cytogenetic locations: 26633544

OMIM:: 604720

Gene summaries Genetic tests Medical literature

Select item 61360912.

*613609 - HOMEOSTATIC IRON REGULATOR; HFE

Cytogenetic locations: 12949720

OMIM:: 613609

Gene summaries Genetic tests Medical literature

Select item 60465313.

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

Cytogenetic locations: contiguous

OMIM:: 604653

Gene summaries Genetic tests Medical literature

Select item 60646414.

*606464 - HEPCIDIN ANTIMICROBIAL PEPTIDE; HAMP

Cytogenetic locations: 17593032

OMIM:: 606464

Gene summaries Genetic tests Medical literature

Select item 31177015.

*311770 - PHOSPHATIDYLINOSITOL GLYCAN ANCHOR BIOSYNTHESIS CLASS A PROTEIN; PIGA

PHOSPHATIDYLINOSITOL GLYCAN ANCHOR BIOSYNTHESIS CLASS A PROTEIN, PSEUDOGENE 1, INCLUDED; PIGAP1, INCLUDED; PIGAP, INCLUDED

Cytogenetic locations: 28081230

OMIM:: 311770

Gene summaries Genetic tests Medical literature

Select item 13477016.

*134770 - FERRITIN HEAVY CHAIN 1; FTH1

Cytogenetic locations: 33162227

OMIM:: 134770

Gene summaries Genetic tests Medical literature

Select item 11226117.

*112261 - BONE MORPHOGENETIC PROTEIN 2; BMP2

REGULATORY ELEMENT, CIS-ACTING, ENHANCER, 110 KB DOWNSTREAM OF BMP2, INCLUDED; RECE-BMP2, INCLUDED

Cytogenetic locations: 13201241

OMIM:: 112261

Gene summaries Genetic tests Medical literature

Select item 22247018.

#222470 - TRICHOHEPATOENTERIC SYNDROME 1; THES1

Cytogenetic locations: 29021008

OMIM:: 222470

Gene summaries Genetic tests Medical literature

Select item 10005019.

100050 - AARSKOG SYNDROME, AUTOSOMAL DOMINANT

OMIM:: 100050

Gene summaries Genetic tests Medical literature

Select item 60574520.

*605745 - CYTOCHROME b REDUCTASE 1; CYBRD1

Cytogenetic locations: 12949720

OMIM:: 605745

Gene summaries Genetic tests Medical literature

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hemochromatosis (75)
OMIM
FOXP2 forkhead box P2 [Homo sapiens]
FOXP2 forkhead box P2 [Homo sapiens]
Gene ID:93986

Gene
OMIM Links for Books (Select 1444528) (2)
OMIM
Gene Links for Books (Select 1444528) (1)
Gene
PMC Links for Books (Select 1444304) (4)
PMC

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