Adrenoleukodystrophy - OMIM - NCBI

Adrenoleukodystrophy - 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 "Adrenoleukodystrophy" 

*601081 - ATP-BINDING CASSETTE, SUBFAMILY 3, MEMBER 2; ABCD2

Cytogenetic locations: 12q12

OMIM:

 

601081

Gene summaries Genetic tests Medical literature

Select item 3003712.

*300371 - ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 1; ABCD1

Cytogenetic locations: Xq28

OMIM:

 

300371

Gene summaries Genetic tests Medical literature

Select item 6015393.

#601539 - PEROXISOME BIOGENESIS DISORDER 1B; PBD1B

Cytogenetic locations: 7q21.2

OMIM:

 

601539

Gene summaries Genetic tests Medical literature

Select item 2644704.

#264470 - PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY

Cytogenetic locations: 17q25.1

OMIM:

 

264470

Gene summaries Genetic tests Medical literature

Select item 3001005.

#300100 - ADRENOLEUKODYSTROPHY; ALD

ADRENOMYELONEUROPATHY, INCLUDED; AMN, INCLUDED

Cytogenetic locations: Xq28

OMIM:

 

300100

Gene summaries Genetic tests Medical literature

Select item 6028596.

*602859 - PEROXISOME BIOGENESIS FACTOR 10; PEX10

Cytogenetic locations: 1p36.32

OMIM:

 

602859

Gene summaries Genetic tests Medical literature

Select item 6021367.

*602136 - PEROXISOME BIOGENESIS FACTOR 1; PEX1

Cytogenetic locations: 7q21.2

OMIM:

 

602136

Gene summaries Genetic tests Medical literature

Select item 6017898.

*601789 - PEROXISOME BIOGENESIS FACTOR 13; PEX13

Cytogenetic locations: 2p15

OMIM:

 

601789

Gene summaries Genetic tests Medical literature

Select item 6086669.

*608666 - PEROXISOME BIOGENESIS FACTOR 26; PEX26

Cytogenetic locations: 22q11.21

OMIM:

 

608666

Gene summaries Genetic tests Medical literature

Select item 31291010.

312910 - SPASTIC PARAPARESIS AND DEAFNESS

OMIM:

 

312910

Gene summaries Genetic tests Medical literature

Select item 21410011.

#214100 - PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER); PBD1A

PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 1, INCLUDED; CG1, INCLUDED

Cytogenetic locations: 7q21.2

OMIM:

 

214100

Gene summaries Genetic tests Medical literature

Select item 30027012.

300270 - ADRENOMYODYSTROPHY

OMIM:

 

300270

Gene summaries Genetic tests Medical literature

Select item 61436213.

*614362 - ACYL-CoA SYNTHETASE, BUBBLEGUM FAMILY, MEMBER 1; ACSBG1

Cytogenetic locations: 15q25.1

OMIM:

 

614362

Gene summaries Genetic tests Medical literature

Select item 61487314.

#614873 - PEROXISOME BIOGENESIS DISORDER 7B; PBD7B

Cytogenetic locations: 22q11.21

OMIM:

 

614873

Gene summaries Genetic tests Medical literature

Select item 27210015.

272100 - SUDANOPHILIC CEREBRAL SCLEROSIS

OMIM:

 

272100

Gene summaries Genetic tests Medical literature

Select item 60321416.

*603214 - ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 4; ABCD4

Cytogenetic locations: 14q24.3

OMIM:

 

603214

Gene summaries Genetic tests Medical literature

Select item 60324717.

*603247 - SOLUTE CARRIER FAMILY 27 (FATTY ACID TRANSPORTER), MEMBER 2; SLC27A2

Cytogenetic locations: 15q21.2

OMIM:

 

603247

Gene summaries Genetic tests Medical literature

Select item 30270018.

302700 - CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE

OMIM:

 

302700

Gene summaries Genetic tests Medical literature

Select item 61486319.

#614863 - PEROXISOME BIOGENESIS DISORDER 4B; PBD4B

Cytogenetic locations: 6p21.1

OMIM:

 

614863

Gene summaries Genetic tests Medical literature

Select item 30047520.

#300475 - DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH

CONTIGUOUS ABCD1/DXS1375E DELETION SYNDROME, INCLUDED; CADDS, INCLUDED

Cytogenetic locations: Xq28

OMIM:

 

300475

Gene summaries Genetic tests Medical literature