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

11/14/2018

gastrointestinal stromal tumor

MONDO_0011719 Condition
GANT
01/14/2020

hypercholesterolemia, autosomal dominant, 3

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

branched-chain keto acid dehydrogenase kinase deficiency

MONDO_0013970 Condition
BCKDK deficiency
01/08/2019

autosomal dominant nonsyndromic deafness

MONDO_0019587 Condition
Autosomal dominant isolated neurosensory deafness type DFNA
07/19/2018

autosomal dominant Ehlers-Danlos syndrome, vascular type

MONDO_0007524 Condition
Ehlers-Danlos syndrome, vascular type, autosomal dominant
08/22/2019

autosomal dominant polycystic kidney disease

MONDO_0004691 Condition
POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
05/22/2019

intellectual disability, autosomal dominant 30

MONDO_0014486 Condition
Mental Retardation, Autosomal Dominant type 30
08/28/2019

intellectual disability, autosomal dominant 22

MONDO_0012869 Condition
Mental Retardation, Autosomal Dominant type 22
08/28/2019

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

parietal foramina 2

MONDO_0012309 Condition
Parietal Foramina type 2
08/13/2019

Gaucher disease perinatal lethal

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

Charcot-Marie-Tooth disease X-linked dominant 1

MONDO_0010549 Condition
CMT1X
01/14/2020

congenital anomaly of kidney and urinary tract

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

intellectual disability, autosomal dominant 5

MONDO_0012960 Condition
Mental Retardation, Autosomal Dominant type 5
08/22/2019

galactokinase deficiency

MONDO_0009255 Condition
Galactosemia II
10/19/2018

multiple intestinal atresia

MONDO_0009465 Condition
CID-MIA/early-onset IBD
10/17/2018

incobotulinumtoxinA

RXNORM:1000104 Drug

Magnesium glycinate

RXNORM:476818 Drug