12q21.32 - OMIM - NCBI

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Items: 13

Select item 6159911.

#615991 - BARDET-BIEDL SYNDROME 14; BBS14

Cytogenetic locations: 1p36, 1p36

OMIM:: 615991

Gene summaries Genetic tests Medical literature

Select item 6101892.

#610189 - SENIOR-LOKEN SYNDROME 6; SLSN6

Cytogenetic locations: 16682973

OMIM:: 610189

Gene summaries Genetic tests Medical literature

Select item 6116643.

#611664 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 7; SHEP7

Cytogenetic locations: 17952075

OMIM:: 611664

Gene summaries Genetic tests Medical literature

Select item 6172554.

#617255 - LISSENCEPHALY 8; LIS8

Cytogenetic locations: Zbtb39

OMIM:: 617255

Gene summaries Genetic tests Medical literature

Select item 6111345.

#611134 - MECKEL SYNDROME, TYPE 4; MKS4

MECKEL-LIKE CEREBRORENODIGITAL SYNDROME, INCLUDED

Cytogenetic locations: 17705300

OMIM:: 611134

Gene summaries Genetic tests Medical literature

Select item 6166976.

#616697 - DEAFNESS, AUTOSOMAL DOMINANT 69; DFNA69

Cytogenetic locations: 26522471

OMIM:: 616697

Gene summaries Genetic tests Medical literature

Select item 6101887.

#610188 - JOUBERT SYNDROME 5; JBTS5

Cytogenetic locations: 16682970

OMIM:: 610188

Gene summaries Genetic tests Medical literature

Select item 6199478.

#619947 - WAARDENBURG SYNDROME, TYPE 2F; WS2F

Cytogenetic locations: 35543077

OMIM:: 619947

Gene summaries Genetic tests Medical literature

Select item 6172189.

*617218 - TRANSMEMBRANE AND TETRATRICOPEPTIDE REPEAT DOMAINS-CONTAINING PROTEIN 3; TMTC3

Cytogenetic locations: Zbtb39

OMIM:: 617218

Gene summaries Genetic tests Medical literature

Select item 14525010.

#145250 - HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE; FPHH

Cytogenetic locations: 15040480

OMIM:: 145250

Gene summaries Genetic tests Medical literature

Select item 61175511.

#611755 - LEBER CONGENITAL AMAUROSIS 10; LCA10

Cytogenetic locations: 38709228

OMIM:: 611755

Gene summaries Genetic tests Medical literature

Select item 61014212.

*610142 - CENTROSOMAL PROTEIN, 290-KD; CEP290

Cytogenetic locations: 16682970

OMIM:: 610142

Gene summaries Genetic tests Medical literature

Select item 18474513.

*184745 - KIT LIGAND; KITLG

Cytogenetic locations: 26522471

OMIM:: 184745

Gene summaries Genetic tests Medical literature

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12q21.32 (13)
OMIM
Central Serous Chorioretinopathy
Central Serous Chorioretinopathy
A visual impairment characterized by the accumulation of fluid under the retina through a defect in the retinal pigment epithelium.<br/>Year introduced: 2010

MeSH

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