Met Results

MET

MET proto-oncogene, receptor tyrosine kinase
01/04/2019

METTL23

methyltransferase like 23
10/16/2018

ADAMTS1

ADAM metallopeptidase with thrombospondin type 1 motif 1

ADAMTS8

ADAM metallopeptidase with thrombospondin type 1 motif 8

GZMM

granzyme M

METAP1

methionyl aminopeptidase 1

METAP1D

methionyl aminopeptidase type 1D, mitochondrial

METAP2

methionyl aminopeptidase 2

METRN

meteorin, glial cell differentiation regulator

METRNL

meteorin like, glial cell differentiation regulator

METTL1

methyltransferase like 1

METTL11B

methyltransferase like 11B

METTL13

methyltransferase like 13

METTL14

methyltransferase like 14

METTL15

methyltransferase like 15

METTL16

methyltransferase like 16

METTL17

methyltransferase like 17

METTL18

methyltransferase like 18

METTL21A

methyltransferase like 21A

METTL21C

methyltransferase like 21C

2-methylbutyryl-CoA dehydrogenase deficiency

MONDO_0012392 Condition
SBCAD deficiency
03/22/2019

03/21/2018

methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency

MONDO_0009612 Condition
Methylmalonyl-CoA mutase deficiency
03/21/2018

vitamin B12-responsive methylmalonic acidemia type cblA

MONDO_0009613 Condition
methylmalonic aciduria, vitamin B12-responsive due to a defect in synthesis of adenosylcobalamin cb1A type
03/21/2018

vitamin B12-responsive methylmalonic acidemia type cblB

MONDO_0009614 Condition
methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type
03/21/2018

guanidinoacetate methyltransferase deficiency

MONDO_0012999 Condition
Cerebral Creatine Deficiency Syndrome type 2
01/25/2019

methylmalonic aciduria and homocystinuria type cblC

MONDO_0010184 Condition
Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblC
11/13/2018

methylmalonic aciduria and homocystinuria type cblD

MONDO_0010185 Condition
Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblD
03/21/2018

10/17/2018

myopathy with abnormal lipid metabolism

MONDO_0009703 Condition
06/12/2018

3-methylglutaconic aciduria type 1

MONDO_0009610 Condition
MGA1
03/08/2019

12/01/2016

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

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

surfactant metabolism dysfunction, pulmonary, 5

MONDO_0013712 Condition
Surfactant Metabolism Dysfunction, Pulmonary, type 5
05/31/2017

10/19/2018

05/31/2017

neurometabolic disorder due to serine deficiency

MONDO_0018162 Condition
Serine deficiency
04/26/2019

metachromatic leukodystrophy, juvenile form

MONDO_0009591 Condition
Arylsulfatase A deficiency, juvenile form
05/31/2017

methemoglobinemia type 4

MONDO_0009605 Condition
10/23/2018

Selenomethionine Se 75

RXNORM:9133 Drug