Lynch syndrome - OMIM - NCBI

Lynch syndrome - 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 "Lynch syndrome" 

#120435 - LYNCH SYNDROME I

LYNCH SYNDROME II, INCLUDED

Cytogenetic locations: 2p21-p16

OMIM:

 

120435

Gene summaries Genetic tests Medical literature

Select item 6002742.

#600274 - FRONTOTEMPORAL DEMENTIA; FTD

PICK COMPLEX, INCLUDED

Cytogenetic locations: 1pter-p36.13, 14q24.2

OMIM:

 

600274

Gene summaries Genetic tests Medical literature

Select item 2036503.

#203650 - ALOPECIA-MENTAL RETARDATION SYNDROME 1; APMR1

Cytogenetic locations: 1pter-p36.13, 3q26.3-q27.3

OMIM:

 

203650

Gene summaries Genetic tests Medical literature

Select item 1454104.

#145410 - OPITZ GBBB SYNDROME, TYPE II; GBBB2

Cytogenetic locations: 22q11.23

OMIM:

 

145410

Gene summaries Genetic tests Medical literature

Select item 6142305.

#614230 - CHROMOSOME 8q21.11 DELETION SYNDROME

Cytogenetic locations: 8q21.11

OMIM:

 

614230

Gene summaries Genetic tests Medical literature

Select item 6067196.

#606719 - MELANOMA-PANCREATIC CANCER SYNDROME

Cytogenetic locations: 9p21.3

OMIM:

 

606719

Gene summaries Genetic tests Medical literature

Select item 6081567.

#608156 - NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS

Cytogenetic locations: 8q22.1

OMIM:

 

608156

Gene summaries Genetic tests Medical literature

Select item 6012288.

#601228 - POLYPOSIS SYNDROME, HEREDITARY MIXED, 1; HMPS1

COLORECTAL CANCER, SUSCEPTIBILITY TO, 4, INCLUDED; CRCS4, INCLUDED

Cytogenetic locations: 15q15.3-q22.1

OMIM:

 

601228

Gene summaries Genetic tests Medical literature

Select item 3082009.

308200 - ICHTHYOSIS AND MALE HYPOGONADISM

RUD SYNDROME, INCLUDED

OMIM:

 

308200

Gene summaries Genetic tests Medical literature

Select item 61088310.

#610883 - POTOCKI-LUPSKI SYNDROME; PTLS

Cytogenetic locations: 17p11.2

OMIM:

 

610883

Gene summaries Genetic tests Medical literature

Select item 61492611.

#614926 - PERRAULT SYNDROME 2; PRLTS2

Cytogenetic locations: 5q31.3

OMIM:

 

614926

Gene summaries Genetic tests Medical literature

Select item 61118512.

%611185 - RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 6; RLS6

Cytogenetic locations: 6p21

OMIM:

 

611185

Gene summaries Genetic tests Medical literature

Select item 60014513.

#600145 - SACRAL DEFECT WITH ANTERIOR MENINGOCELE

CAUDAL DYSGENESIS SYNDROME, INCLUDED

Cytogenetic locations: 1p13.1

OMIM:

 

600145

Gene summaries Genetic tests Medical literature

Select item 15340014.

#153400 - LYMPHEDEMA-DISTICHIASIS SYNDROME

LYMPHEDEMA-DISTICHIASIS SYNDROME WITH RENAL DISEASE AND DIABETES MELLITUS, INCLUDED

Cytogenetic locations: 16q24.1

OMIM:

 

153400

Gene summaries Genetic tests Medical literature

Select item 60615615.

606156 - SENER SYNDROME

OMIM:

 

606156

Gene summaries Genetic tests Medical literature

Select item 61702216.

#617022 - LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10

Cytogenetic locations: 14q24.3

OMIM:

 

617022

Gene summaries Genetic tests Medical literature

Select item 15832017.

#158320 - MUIR-TORRE SYNDROME; MRTES

Cytogenetic locations: 1pter-p36.13, 2p21-p16

OMIM:

 

158320

Gene summaries Genetic tests Medical literature

Select item 60736418.

#607364 - BARTTER SYNDROME, TYPE 3; BARTS3

BARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED

Cytogenetic locations: 1p36.13

OMIM:

 

607364

Gene summaries Genetic tests Medical literature

Select item 17645019.

#176450 - CURRARINO SYNDROME

SACRAL AGENESIS SYNDROME, INCLUDED

Cytogenetic locations: 7q36.3

OMIM:

 

176450

Gene summaries Genetic tests Medical literature

Select item 61285320.

%612853 - RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 7; RLS7

Cytogenetic locations: 2p14-p13

OMIM:

 

612853

Gene summaries Genetic tests Medical literature