Anemia - OMIM - NCBI

Anemia - OMIM - NCBI

Anemia

- HLBS-PopOmics -

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 "Anemia" 

206000 - ANEMIA, SIDEROBLASTIC, PYRIDOXINE-RESPONSIVE, AUTOSOMAL RECESSIVE

OMIM:

 

206000

Gene summaries Genetic tests Medical literature

Select item 1028002.

%102800 - ADENOSINE TRIPHOSPHATASE DEFICIENCY, ANEMIA DUE TO

OMIM:

 

102800

Gene summaries Genetic tests Medical literature

Select item 2057003.

205700 - ANEMIA, AUTOIMMUNE HEMOLYTIC

OMIM:

 

205700

Gene summaries Genetic tests Medical literature

Select item 2478004.

%247800 - LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNE HEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS

OMIM:

 

247800

Gene summaries Genetic tests Medical literature

Select item 2063005.

206300 - ANEMIA, NONSPHEROCYTIC HEMOLYTIC, ASSOCIATED WITH ABNORMALITY OF RED CELL MEMBRANE

OMIM:

 

206300

Gene summaries Genetic tests Medical literature

Select item 2661206.

#266120 - URIDINE 5-PRIME MONOPHOSPHATE HYDROLASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO

Cytogenetic locations: 7p14.3

OMIM:

 

266120

Gene summaries Genetic tests Medical literature

Select item 6043157.

604315 - ANEMIA, CONGENITAL HYPOPLASTIC, WITH MULTIPLE CONGENITAL ANOMALIES/MENTAL RETARDATION SYNDROME

OMIM:

 

604315

Gene summaries Genetic tests Medical literature

Select item 2353708.

235370 - HEMOLYTIC ANEMIA WITH THERMAL SENSITIVITY OF RED CELLS

OMIM:

 

235370

Gene summaries Genetic tests Medical literature

Select item 2064009.

206400 - ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRIN METABOLISM

OMIM:

 

206400

Gene summaries Genetic tests Medical literature

Select item 60727910.

%607279 - SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1; SLEH1

Cytogenetic locations: 11q14

OMIM:

 

607279

Gene summaries Genetic tests Medical literature

Select item 60046111.

600461 - HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES

OMIM:

 

600461

Gene summaries Genetic tests Medical literature

Select item 60346712.

#603467 - FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF

Cytogenetic locations: 11p14.3

OMIM:

 

603467

Gene summaries Genetic tests Medical literature

Select item 17090013.

170900 - PERNICIOUS ANEMIA

OMIM:

 

170900

Gene summaries Genetic tests Medical literature

Select item 10560014.

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

Cytogenetic locations: 15q21

OMIM:

 

105600

Gene summaries Genetic tests Medical literature

Select item 21972115.

219721 - CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION

OMIM:

 

219721

Gene summaries Genetic tests Medical literature

Select item 61740916.

#617409 - DIAMOND-BLACKFAN ANEMIA 17; DBA17

Cytogenetic locations: 1q21.3

OMIM:

 

617409

Gene summaries Genetic tests Medical literature

Select item 61740817.

#617408 - DIAMOND-BLACKFAN ANEMIA 16; DBA16

Cytogenetic locations: 17q21.31

OMIM:

 

617408

Gene summaries Genetic tests Medical literature

Select item 14170018.

141700 - HEMOLYTIC POIKILOCYTIC ANEMIA DUE TO REDUCED ANKYRIN BINDING SITES

OMIM:

 

141700

Gene summaries Genetic tests Medical literature

Select item 61130119.

*611301 - CHROMOSOME 17 OPEN READING FRAME 70; C17ORF70

Cytogenetic locations: 17q25.3

OMIM:

 

611301

Gene summaries Genetic tests Medical literature

Select item 60612920.

%606129 - DIAMOND-BLACKFAN ANEMIA 2; DBA2

Cytogenetic locations: 8p23.3-p22

OMIM:

 

606129

Gene summaries Genetic tests Medical literature