Ina Results

SERPINA1

serpin family A member 1
05/02/2018

NFKBIZ

NFKB inhibitor zeta
07/10/2017

AK6

adenylate kinase 6

APBB1IP

amyloid beta precursor protein binding family B member 1 interacting protein

ASIC5

acid sensing ion channel subunit family member 5

CALHM6

calcium homeostasis modulator family member 6

CARD8

caspase recruitment domain family member 8

CFI

complement factor I

GRINA

glutamate ionotropic receptor NMDA type subunit associated protein 1

INA

internexin neuronal intermediate filament protein alpha

INAFM1

InaF motif containing 1

INAFM2

InaF motif containing 2

INAVA

innate immunity activator

ITGAE

integrin subunit alpha E

KDM2A

lysine demethylase 2A

RIOX2

ribosomal oxygenase 2

SERPINA10

serpin family A member 10

SERPINA11

serpin family A member 11

SERPINA12

serpin family A member 12

autosomal dominant nonsyndromic deafness

MONDO_0019587 Condition
Autosomal dominant isolated neurosensory deafness type DFNA

hypercholesterolemia, autosomal dominant, 3

MONDO_0011369 Condition
Hypercholesterolemia, Autosomal Dominant, type 3
05/21/2018

autosomal dominant Ehlers-Danlos syndrome, vascular type

MONDO_0007524 Condition
Ehlers-Danlos syndrome, vascular type, autosomal dominant
01/10/2018

05/21/2018

branched-chain keto acid dehydrogenase kinase deficiency

MONDO_0013970 Condition
BCKDK deficiency
01/08/2019

intellectual disability, autosomal dominant 30

MONDO_0014486 Condition
Mental Retardation, Autosomal Dominant type 30
03/28/2018

intellectual disability, autosomal dominant 3

MONDO_0012946 Condition
Mental Retardation, Autosomal Dominant type 3
05/31/2017

01/10/2018

parietal foramina 2

MONDO_0012309 Condition
Parietal Foramina type 2
06/01/2017

autosomal dominant cerebellar ataxia, deafness and narcolepsy

MONDO_0011397 Condition
ADCA-DN syndrome
02/10/2017

Charcot-Marie-Tooth disease dominant intermediate b

MONDO_0011674 Condition
DI-CMTB
02/05/2018

Gaucher disease perinatal lethal

MONDO_0011945 Condition
Gaucher Disease, Collodion Type
01/10/2018

autosomal dominant nonsyndromic deafness 70

MONDO_0014853 Condition
Deafness, Autosomal Dominant 70
01/04/2018

autosomal dominant nonsyndromic deafness 66

MONDO_0014854 Condition
Deafness, Autosomal Dominant 66
03/20/2018

intellectual disability, autosomal dominant 43

MONDO_0014858 Condition
MRD43
04/25/2018

heterotopia, periventricular, X-linked dominant

MONDO_0010233 Condition
Heterotopia, Periventricular, Ehlers-Danlos Variant
06/01/2017

glycogen storage disease due to phosphoglycerate kinase 1 deficiency

MONDO_0010392 Condition
GSD due to phosphoglycerate kinase 1 deficiency
06/13/2017

congenital anomaly of kidney and urinary tract

MONDO_0019719 Condition
Congenital anomalies of kidney and urinary tract
11/18/2016

incobotulinumtoxinA

RXNORM:1000104 Drug

Magnesium glycinate

RXNORM:476818 Drug