Aging - OMIM - NCBI

Aging - 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 "Aging" 

601811 - PREMATURE AGING SYNDROME, OKAMOTO TYPE

OMIM:

 

601811

Gene summaries Genetic tests Medical literature

Select item 6174372.

*617437 - S100 CALCIUM-BINDING PROTEIN A16; S100A16

Cytogenetic locations: 1q21.3

OMIM:

 

617437

Gene summaries Genetic tests Medical literature

Select item 5020003.

#502000 - AGING

OMIM:

 

502000

Gene summaries Genetic tests Medical literature

Select item 6018124.

#601812 - PREMATURE AGING SYNDROME, PENTTINEN TYPE; PENTT

Cytogenetic locations: 5q32

OMIM:

 

601812

Gene summaries Genetic tests Medical literature

Select item 1136205.

#113620 - BRANCHIOOCULOFACIAL SYNDROME; BOFS

Cytogenetic locations: 6p24.3

OMIM:

 

113620

Gene summaries Genetic tests Medical literature

Select item 1047606.

*104760 - AMYLOID BETA A4 PRECURSOR PROTEIN; APP

Cytogenetic locations: 21q21.3

OMIM:

 

104760

Gene summaries Genetic tests Medical literature

Select item 1734107.

*173410 - PLATELET-DERIVED GROWTH FACTOR RECEPTOR, BETA; PDGFRB

PDGFRB/ETV6 FUSION GENE, INCLUDED

Cytogenetic locations: 5q32

OMIM:

 

173410

Gene summaries Genetic tests Medical literature

Select item 6013498.

%601349 - MICROPHTHALMIA, SYNDROMIC 8; MCOPS8

Cytogenetic locations: 6q21

OMIM:

 

601349

Gene summaries Genetic tests Medical literature

Select item 6159199.

#615919 - ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2

Cytogenetic locations: 20p12.3

OMIM:

 

615919

Gene summaries Genetic tests Medical literature

Select item 61734110.

#617341 - CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2; CRMCC2

Cytogenetic locations: 10q24.33

OMIM:

 

617341

Gene summaries Genetic tests Medical literature

Select item 17667011.

#176670 - HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS

PROGERIA SYNDROME, CHILDHOOD-ONSET, INCLUDED

OMIM:

 

176670

Gene summaries Genetic tests Medical literature

Select item 10927012.

+109270 - SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1

ACANTHOCYTOSIS, ONE FORM OF, INCLUDED

Cytogenetic locations: 17q21.31

OMIM:

 

109270

Gene summaries Genetic tests Medical literature

Select item 19405013.

#194050 - WILLIAMS-BEUREN SYNDROME; WBS

Cytogenetic locations: 7q11.23

OMIM:

 

194050

Gene summaries Genetic tests Medical literature

Select item 15033014.

*150330 - LAMIN A/C; LMNA

LAMIN A, INCLUDED

Cytogenetic locations: 1q22

OMIM:

 

150330

Gene summaries Genetic tests Medical literature

Select item 60378015.

*603780 - RECQ PROTEIN-LIKE 4; RECQL4

Cytogenetic locations: 8q24.3

OMIM:

 

603780

Gene summaries Genetic tests Medical literature

Select item 60350516.

*603505 - CELL DIVISION CYCLE 14, S. CEREVISIAE, HOMOLOG B; CDC14B

Cytogenetic locations: 9q22.32-q22.33

OMIM:

 

603505

Gene summaries Genetic tests Medical literature

Select item 60819617.

*608196 - WERNER HELICASE-INTERACTING PROTEIN 1; WRNIP1

Cytogenetic locations: 6p25.2

OMIM:

 

608196

Gene summaries Genetic tests Medical literature

Select item 61096518.

#610965 - XFE PROGEROID SYNDROME; XFEPS

Cytogenetic locations: 16p13.12

OMIM:

 

610965

Gene summaries Genetic tests Medical literature

Select item 60024119.

*600241 - G PROTEIN-COUPLED RECEPTOR 3; GPR3

Cytogenetic locations: 1p36.11

OMIM:

 

600241

Gene summaries Genetic tests Medical literature

Select item 10872520.

%108725 - ATHEROSCLEROSIS SUSCEPTIBILITY; ATHS

Cytogenetic locations: 19p13.3-p13.2

OMIM:

 

108725

Gene summaries Genetic tests Medical literature