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Title : Education - OMIM - NCBI
link : Education - OMIM - NCBI

Education - OMIM - NCBI

Education - 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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*602228 - TRANSCRIPTION FACTOR 7-LIKE 2; TCF7L2

TCF7L2/VTI1A FUSION GENE, INCLUDED

Cytogenetic locations: 10q25.2-q25.3

OMIM:

 

602228

Gene summaries Genetic tests Medical literature

Select item 1055002.

#105500 - AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1

Cytogenetic locations: 15q21.2

OMIM:

 

105500

Gene summaries Genetic tests Medical literature

Select item 6157523.

#615752 - POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE; BPPR

Cytogenetic locations: 16q21

OMIM:

 

615752

Gene summaries Genetic tests Medical literature

Select item 6156024.

#615602 - MEMORY QUANTITATIVE TRAIT LOCUS; MEMRYQTL

Cytogenetic locations: 5q34

OMIM:

 

615602

Gene summaries Genetic tests Medical literature

Select item 6068965.

%606896 - DYSLEXIA, SUSCEPTIBILITY TO, 5; DYX5

Cytogenetic locations: 3p12-q13

OMIM:

 

606896

Gene summaries Genetic tests Medical literature

Select item 6136036.

#613603 - CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME

Cytogenetic locations: 4q32.1-q32.2

OMIM:

 

613603

Gene summaries Genetic tests Medical literature

Select item 6093077.

#609307 - SPINOCEREBELLAR ATAXIA 27; SCA27

Cytogenetic locations: 13q33.1

OMIM:

 

609307

Gene summaries Genetic tests Medical literature

Select item 1078008.

107800 - ARCUS CORNEAE

OMIM:

 

107800

Gene summaries Genetic tests Medical literature

Select item 6089089.

#608908 - MYOPIA 6; MYP6

Cytogenetic locations: 22q13.33

OMIM:

 

608908

Gene summaries Genetic tests Medical literature

Select item 61610810.

#616108 - RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS

Cytogenetic locations: 14q24.1

OMIM:

 

616108

Gene summaries Genetic tests Medical literature

Select item 61686311.

#616863 - CHROMOSOME 16p13.2 DELETION SYNDROME

Cytogenetic locations: 16p13.2

OMIM:

 

616863

Gene summaries Genetic tests Medical literature

Select item 61480712.

#614807 - MYOPATHY, CENTRONUCLEAR, 4; CNM4

Cytogenetic locations: 16p13.3

OMIM:

 

614807

Gene summaries Genetic tests Medical literature

Select item 61466613.

*614666 - COILED-COIL DOMAIN-CONTAINING PROTEIN 78; CCDC78

Cytogenetic locations: 16p13.3

OMIM:

 

614666

Gene summaries Genetic tests Medical literature

Select item 30084814.

%300848 - MENTAL RETARDATION, X-LINKED 89; MRX89

Cytogenetic locations: Xp11.3

OMIM:

 

300848

Gene summaries Genetic tests Medical literature

Select item 61783115.

#617831 - MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55

Cytogenetic locations: 6q22.1

OMIM:

 

617831

Gene summaries Genetic tests Medical literature

Select item 61053316.

*610533 - WW, C2, AND COILED-COIL DOMAIN-CONTAINING 1; WWC1

Cytogenetic locations: 5q34

OMIM:

 

610533

Gene summaries Genetic tests Medical literature

Select item 61553817.

#615538 - CHROMOSOME 22q13 DUPLICATION SYNDROME

Cytogenetic locations: 22q13

OMIM:

 

615538

Gene summaries Genetic tests Medical literature

Select item 30012318.

#300123 - MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISM

MENTAL RETARDATION, X-LINKED, WITH ISOLATED GROWTH HORMONE DEFICIENCY, INCLUDED; MRGH, INCLUDED

Cytogenetic locations: Xq27.1

OMIM:

 

300123

Gene summaries Genetic tests Medical literature

Select item 61738419.

#617384 - HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4

Cytogenetic locations: 10q21.3

OMIM:

 

617384

Gene summaries Genetic tests Medical literature

Select item 31499520.

*314995 - ZINC FINGER PROTEIN 41; ZNF41

Cytogenetic locations: Xp11.3

OMIM:

 

314995

Gene summaries Genetic tests Medical literature

Thus Article Education - OMIM - NCBI

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