Gh Results

MED12

mediator complex subunit 12
10/10/2018

CASK

calcium/calmodulin dependent serine protein kinase
09/11/2017

FOXP2

forkhead box P2
10/10/2018

IGHMBP2

immunoglobulin mu DNA binding protein 2
10/22/2018

SNAI2

snail family transcriptional repressor 2
08/23/2018

ARID3A

AT-rich interaction domain 3A

CELF3

CUGBP Elav-like family member 3

DLG1

discs large MAGUK scaffold protein 1

EP400

E1A binding protein p400

GGH

gamma-glutamyl hydrolase

GH1

growth hormone 1

GH2

growth hormone 2

GHDC

GH3 domain containing

GHITM

growth hormone inducible transmembrane protein

GHR

growth hormone receptor

GHRH

growth hormone releasing hormone

GHRHR

growth hormone releasing hormone receptor

GHRL

ghrelin and obestatin prepropeptide

GHSR

growth hormone secretagogue receptor

GTPBP10

GTP binding protein 10

Leigh syndrome

MONDO_0009723 Condition

arrhythmogenic right ventricular dysplasia 9

MONDO_0012180 Condition
arrhythmogenic right ventricular cardiomyopathy 9
10/23/2017

Peutz-Jeghers syndrome

MONDO_0008280 Condition
Polyps and spots syndrome
01/07/2019

arrhythmogenic right ventricular dysplasia 11

MONDO_0012506 Condition
Arrhythmogenic Right Ventricular Dysplasia, Familial, type 11
01/07/2019

Chudley-McCullough syndrome

MONDO_0011411 Condition
10/22/2018

arrhythmogenic right ventricular dysplasia 8

MONDO_0011831 Condition
Arrhythmogenic Right Ventricular Dysplasia, Familial, type 8
10/23/2017

congenital stationary night blindness 1E

MONDO_0013807 Condition
CSNB1E
10/16/2018

congenital stationary night blindness 1A

MONDO_0010690 Condition
congenital stationary night blindness type 1A
05/31/2017

03/20/2018

arrhythmogenic right ventricular dysplasia 10

MONDO_0012434 Condition
Arrhythmogenic Right Ventricular Dysplasia, Familial, type 10
10/23/2017

congenital stationary night blindness 1D

MONDO_0013450 Condition
CSNB1D
10/16/2018

congenital stationary night blindness 1C

MONDO_0013183 Condition
congenital stationary night blindness 1C autosomal recessive
06/01/2017

leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome

MONDO_0013971 Condition
Combined oxidative phosphorylation defect type 12
10/17/2018

10/17/2018

arrhythmogenic right ventricular dysplasia 5

MONDO_0011459 Condition
arrhythmogenic right ventricular cardiomyopathy 5
10/23/2017

Leigh disease

MONDO_0018859 Condition
Infantile subacute necrotizing encephalopathy

3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome

MONDO_0013875 Condition
3-methylglutaconic aciduria type 6
05/31/2017

congenital stationary night blindness 1B

MONDO_0009758 Condition
CSNB1B
10/15/2018

arrhythmogenic right ventricular dysplasia 12

MONDO_0012684 Condition
Arrhythmogenic Right Ventricular Dysplasia, Familial, type 12

rough marshelder pollen extract

RXNORM:852532 Drug

ColdCough PD

RXNORM:801156 Drug

Enlighten Me!

RXNORM:1043713 Drug