Octahydro-5-(2-octyldecyl)-4,7-methano-1H-indene - OMIM - NCBI

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Items: 14

The following terms were not found in OMIM: Octahydro, Octahydro-5-, octyldecyl, 2-octyldecyl, methano, indene, 7-methano-1H-indene.

Select item 6079041.

*607904 - CALCIUM CHANNEL, VOLTAGE-DEPENDENT, T TYPE, ALPHA-1H SUBUNIT; CACNA1H

Cytogenetic locations: 12853961

OMIM:: 607904

Gene summaries Genetic tests Medical literature

Select item 1393902.

*139390 - GUANINE NUCLEOTIDE-BINDING PROTEIN, BETA-2; GNB2

Cytogenetic locations: 12853961

OMIM:: 139390

Gene summaries Genetic tests Medical literature

Select item 6045803.

*604580 - FIBULIN 5; FBLN5

Cytogenetic locations: 11805834

OMIM:: 604580

Gene summaries Genetic tests Medical literature

Select item 6015484.

*601548 - EGF-CONTAINING FIBULIN-LIKE EXTRACELLULAR MATRIX PROTEIN 1; EFEMP1

Cytogenetic locations: 30541486

OMIM:: 601548

Gene summaries Genetic tests Medical literature

Select item 1343705.

*134370 - COMPLEMENT FACTOR H; CFH

FACTOR H-LIKE 1, INCLUDED; FHL1, INCLUDED

Cytogenetic locations: PDC

OMIM:: 134370

Gene summaries Genetic tests Medical literature

Select item 2756306.

#275630 - CHANARIN-DORFMAN SYNDROME; CDS

Cytogenetic locations: 13993689

OMIM:: 275630

Gene summaries Genetic tests Medical literature

Select item 1141837.

*114183 - CALMODULIN 3; CALM3

Cytogenetic locations: 31454269

OMIM:: 114183

Gene summaries Genetic tests Medical literature

Select item 1563508.

*156350 - METALLOTHIONEIN 1A; MT1A

Cytogenetic locations: 602389

OMIM:: 156350

Gene summaries Genetic tests Medical literature

Select item 1415009.

#141500 - MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1

MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA, INCLUDED

Cytogenetic locations: 15311627

OMIM:: 141500

Gene summaries Genetic tests Medical literature

Select item 60823010.

*608230 - CALCIUM CHANNEL, VOLTAGE-DEPENDENT, T TYPE, ALPHA-1I SUBUNIT; CACNA1I

Cytogenetic locations: Radial

OMIM:: 608230

Gene summaries Genetic tests Medical literature

Select item 60406511.

*604065 - CALCIUM CHANNEL, VOLTAGE-DEPENDENT, T TYPE, ALPHA-1G SUBUNIT; CACNA1G

Cytogenetic locations: 29495342

OMIM:: 604065

Gene summaries Genetic tests Medical literature

Select item 30052312.

#300523 - ALLAN-HERNDON-DUDLEY SYNDROME; AHDS

Cytogenetic locations: 300433

OMIM:: 300523

Gene summaries Genetic tests Medical literature

Select item 23540013.

#235400 - HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1

HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED

Cytogenetic locations: Gastrointestinal, 1p36, PDC

OMIM:: 235400

Gene summaries Genetic tests Medical literature

Select item 60981414.

#609814 - COMPLEMENT FACTOR H DEFICIENCY; CFHD

Cytogenetic locations: PDC

OMIM:: 609814

Gene summaries Genetic tests Medical literature

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Octahydro-5- AND (2-octyldecyl) AND -4,7-methano-1H-indene (14)
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