Methyl 17,20-acetonidodihydroprednisolonate - OMIM - NCBI

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The following terms were not found in OMIM: acetonidodihydroprednisolonate, 20-acetonidodihydroprednisolonate.

Select item 3000051.

*300005 - METHYL-CpG-BINDING PROTEIN 2; MECP2

Cytogenetic locations: -

OMIM:: 300005

Gene summaries Genetic tests Medical literature

Select item 6152622.

*615262 - METHYLTRANSFERASE-LIKE 23; METTL23

Cytogenetic locations: 32439618

OMIM:: 615262

Gene summaries Genetic tests Medical literature

Select item 2428603.

#242860 - IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1; ICF1

Cytogenetic locations: 20p13

OMIM:: 242860

Gene summaries Genetic tests Medical literature

Select item 6055504.

*605550 - RAS PROTEIN, DEXAMETHASONE-INDUCED, 1; RASD1

Cytogenetic locations: 10673050

OMIM:: 605550

Gene summaries Genetic tests Medical literature

Select item 6045115.

*604511 - CHROMOBOX 1; CBX1

Cytogenetic locations: 17470536

OMIM:: 604511

Gene summaries Genetic tests Medical literature

Select item 6018606.

*601860 - 17-@BETA-HYDROXYSTEROID DEHYDROGENASE IV; HSD17B4

Cytogenetic locations: 611648

OMIM:: 601860

Gene summaries Genetic tests Medical literature

Select item 1137057.

*113705 - BRCA1 DNA REPAIR-ASSOCIATED PROTEIN; BRCA1

Cytogenetic locations: 21901007

OMIM:: 113705

Gene summaries Genetic tests Medical literature

Select item 6133458.

#613345 - HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2; HOKPP2

Cytogenetic locations: 15557532

OMIM:: 613345

Gene summaries Genetic tests Medical literature

Select item 1225619.

*122561 - CORTICOTROPIN-RELEASING HORMONE RECEPTOR 1; CRHR1

Cytogenetic locations: 12399950

OMIM:: 122561

Gene summaries Genetic tests Medical literature

Select item 61102010.

*611020 - MICRO RNA 21; MIR21

Cytogenetic locations: 17363372

OMIM:: 611020

Gene summaries Genetic tests Medical literature

Select item 60288711.

*602887 - DISCS LARGE MAGUK SCAFFOLD PROTEIN 4; DLG4

Cytogenetic locations: 12609736

OMIM:: 602887

Gene summaries Genetic tests Medical literature

Select item 61591712.

#615917 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20; COXPD20

Cytogenetic locations: 25058219

OMIM:: 615917

Gene summaries Genetic tests Medical literature

Select item 60396713.

*603967 - SODIUM VOLTAGE-GATED CHANNEL, ALPHA SUBUNIT 4; SCN4A

Cytogenetic locations: 26700687

OMIM:: 603967

Gene summaries Genetic tests Medical literature

Select item 16860014.

#168600 - PARKINSON DISEASE, LATE-ONSET; PD

Cytogenetic locations: 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 1p36

OMIM:: 168600

Gene summaries Genetic tests Medical literature

Select item 18024015.

*180240 - RETINOIC ACID RECEPTOR, ALPHA; RARA

ACUTE PROMYELOCYTIC LEUKEMIA BREAKPOINT CLUSTER REGION, INCLUDED

Cytogenetic locations: 10610177

OMIM:: 180240

Gene summaries Genetic tests Medical literature

Select item 10257816.

*102578 - ACUTE PROMYELOCYTIC LEUKEMIA, INDUCER OF; PML

PML/RARA FUSION GENE, INCLUDED

Cytogenetic locations: 1p36, 1p36

OMIM:: 102578

Gene summaries Genetic tests Medical literature

Select item 31275017.

#312750 - RETT SYNDROME; RTT

RETT SYNDROME, ZAPPELLA VARIANT, INCLUDED

Cytogenetic locations: -

OMIM:: 312750

Gene summaries Genetic tests Medical literature

Select item 15620018.

#156200 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 1; MRD1

CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED

Cytogenetic locations: 19904302

OMIM:: 156200

Gene summaries Genetic tests Medical literature

Select item 30026019.

#300260 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL

Cytogenetic locations: -

OMIM:: 300260

Gene summaries Genetic tests Medical literature

Select item 30074620.

*300746 - COAGULATION FACTOR IX; F9

Cytogenetic locations: CHRDL1

OMIM:: 300746

Gene summaries Genetic tests Medical literature

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Methyl 17,20-acetonidodihydroprednisolonate (63)
OMIM
20844[HGNC] (75)
ClinVar
otor[All Fields] AND 1[has_clinical] (28)
dbVar

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