chrysanthemyl diphosphate synthase - OMIM - NCBI

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The following term was not found in OMIM: chrysanthemyl.

Select item 6105641.

*610564 - PRENYL DIPHOSPHATE SYNTHASE, SUBUNIT 2; PDSS2

Cytogenetic locations: 616842

OMIM:: 610564

Gene summaries Genetic tests Medical literature

Select item 6012912.

*601291 - URIDINE DIPHOSPHATE GLYCOSYLTRANSFERASE 8; UGT8

Cytogenetic locations: P#cX##

OMIM:: 601291

Gene summaries Genetic tests Medical literature

Select item 6074293.

*607429 - PRENYL DIPHOSPHATE SYNTHASE, SUBUNIT 1; PDSS1

Cytogenetic locations: Sephs1

OMIM:: 607429

Gene summaries Genetic tests Medical literature

Select item 1346294.

*134629 - FARNESYL DIPHOSPHATE SYNTHASE; FDPS

OMIM:: 134629

Gene summaries Genetic tests Medical literature

Select item 6081725.

*608172 - DEHYDRODOLICHYL DIPHOSPHATE SYNTHASE; DHDDS

Cytogenetic locations: ######

OMIM:: 608172

Gene summaries Genetic tests Medical literature

Select item 6069826.

*606982 - GERANYLGERANYL DIPHOSPHATE SYNTHASE 1; GGPS1

OMIM:: 606982

Gene summaries Genetic tests Medical literature

Select item 6104637.

*610463 - NUS1 DEHYDRODOLICHYL DIPHOSPHATE SYNTHASE SUBUNIT; NUS1

OMIM:: 610463

Gene summaries Genetic tests Medical literature

Select item 6040558.

*604055 - ISOPENTENYL-DIPHOSPHATE DELTA ISOMERASE 1; IDI1

OMIM:: 604055

Gene summaries Genetic tests Medical literature

Select item 6181569.

#618156 - SQUALENE SYNTHASE DEFICIENCY; SQSD

Cytogenetic locations: ######

OMIM:: 618156

Gene summaries Genetic tests Medical literature

Select item 60815210.

*608152 - PROSTAGLANDIN E SYNTHASE 2; PTGES2

Cytogenetic locations: 184757

OMIM:: 608152

Gene summaries Genetic tests Medical literature

Select item 61465211.

#614652 - COENZYME Q10 DEFICIENCY, PRIMARY, 3; COQ10D3

Cytogenetic locations: CCNC

OMIM:: 614652

Gene summaries Genetic tests Medical literature

Select item 61663112.

#616631 - POROKERATOSIS 9, MULTIPLE TYPES; POROK9

OMIM:: 616631

Gene summaries Genetic tests Medical literature

Select item 61386113.

#613861 - RETINITIS PIGMENTOSA 59; RP59

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ibb, INCLUDED; CDG1BB, INCLUDED

Cytogenetic locations: 03.<##

OMIM:: 613861

Gene summaries Genetic tests Medical literature

Select item 61783614.

#617836 - DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM

OMIM:: 617836

Gene summaries Genetic tests Medical literature

Select item 61465115.

#614651 - COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2

Cytogenetic locations: ###?##

OMIM:: 614651

Gene summaries Genetic tests Medical literature

Select item 61708216.

#617082 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iaa; CDG1AA

OMIM:: 617082

Gene summaries Genetic tests Medical literature

Select item 61783117.

#617831 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55

Cytogenetic locations: @##\##

OMIM:: 617831

Gene summaries Genetic tests Medical literature

Select item 61951818.

#619518 - MUSCULAR DYSTROPHY, CONGENITAL HEARING LOSS, AND OVARIAN INSUFFICIENCY SYNDROME; MDHLO

Cytogenetic locations: ##T###

OMIM:: 619518

Gene summaries Genetic tests Medical literature

Select item 25600019.

#256000 - LEIGH SYNDROME; LS

OMIM:: 256000

Gene summaries Genetic tests Medical literature

Select item 61161020.

*611610 - PHOSPHOGLUCOMUTASE 2-LIKE 1; PGM2L1

OMIM:: 611610

Gene summaries Genetic tests Medical literature

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