Ar Results

RYR2

ryanodine receptor 2
04/02/2018

ARHGEF6

Rac/Cdc42 guanine nucleotide exchange factor 6
10/10/2018

SMARCA4

SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
01/07/2019

PCSK9

proprotein convertase subtilisin/kexin type 9
05/21/2018

AARS

alanyl-tRNA synthetase
11/20/2018

ARID1B

AT-rich interaction domain 1B
12/04/2019

ARHGEF9

Cdc42 guanine nucleotide exchange factor 9
11/21/2019

ARG1

arginase 1
10/18/2018

FARS2

phenylalanyl-tRNA synthetase 2, mitochondrial
11/25/2019

CDKN2A

cyclin dependent kinase inhibitor 2A
08/14/2019

TSPEAR

thrombospondin type laminin G domain and EAR repeats
11/09/2018

SMARCB1

SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
08/22/2019

BSND

barttin CLCNK type accessory beta subunit
07/12/2018

BARD1

BRCA1 associated RING domain 1
08/09/2017

ARX

aristaless related homeobox
12/05/2019

NSD1

nuclear receptor binding SET domain protein 1
08/13/2019

MARVELD2

MARVEL domain containing 2
10/16/2018

KARS

lysyl-tRNA synthetase
10/17/2018

FXN

frataxin
10/16/2018

AR

androgen receptor
08/14/2019

hypertrophic cardiomyopathy

MONDO_0005045 Condition
Obstructive hypertrophic cardiomyopathy
08/06/2018

hereditary breast carcinoma

MONDO_0016419 Condition
Hereditary Breast Carcinoma
01/10/2018

familial ovarian cancer

MONDO_0016248 Condition
Familial ovarian malignant tumor
01/10/2018

cardiofaciocutaneous syndrome

MONDO_0015280 Condition
CFC syndrome
07/24/2018

hereditary nonpolyposis colon cancer

MONDO_0018630 Condition
Familial nonpolyposis colon cancer
10/12/2018

undetermined early-onset epileptic encephalopathy

MONDO_0018614 Condition
Undetermined EOEE
01/17/2019

early infantile epileptic encephalopathy

MONDO_0016021 Condition
Early Infantile Epileptic Encephalopathy with Burst-Suppression
10/25/2019

nevoid basal cell carcinoma syndrome

MONDO_0007187 Condition
Nevoid basal cell carcinoma syndrome
08/13/2019

aneurysm-osteoarthritis syndrome

MONDO_0013426 Condition
Loeys-Dietz Syndrome type 3
08/22/2019

hereditary diffuse gastric adenocarcinoma

MONDO_0007648 Condition
Hereditary Diffuse Gastric Cancer
08/22/2019

Marfan syndrome

MONDO_0007947 Condition
MFS1
12/04/2019

hypertrophic cardiomyopathy 10

MONDO_0012112 Condition
Cardiomyopathy, Familial Hypertrophic, type 10
01/11/2018

06/01/2017

hyperparathyroidism-jaw tumor syndrome

MONDO_0007768 Condition
Hyperparathyroidism-2
04/19/2019

glutaryl-CoA dehydrogenase deficiency

MONDO_0009281 Condition
Glutaric aciduria type 1
11/08/2019

Bernard-Soulier syndrome

MONDO_0009276 Condition
Giant platelet syndrome
11/27/2019

08/28/2019

arrhythmogenic right ventricular dysplasia 9

MONDO_0012180 Condition
arrhythmogenic right ventricular cardiomyopathy 9
08/22/2019

breast-ovarian cancer, familial, susceptibility to, 2

MONDO_0012933 Condition
Breast-Ovarian Cancer, Familial, Susceptibility To, type 2
08/22/2019

ornithine carbamoyltransferase deficiency

MONDO_0010703 Condition
Ornithine carbamoyltransferase deficiency
10/29/2019

Ferrous fumarate 189 MG

RXNORM:852774 Drug

Aloe vera preparation 470 MG

RXNORM:577867 Drug