Search results for 3-Methylcrotonylglycine

40 hits were found for 3-Methylcrotonylglycine

# Family MCID Name MIFTS Score
1
3MT008 3-Methylcrotonyl-Coa Carboxylase 2 Deficiency 31 4.301
2
3MT011 3-Methylcrotonyl-Coa Carboxylase 1 Deficiency 38 3.055
3
3MT001 3-Methylcrotonyl-Coa Carboxylase Deficiency 52 2.553
4
P HYP265 Hypotonia 42 1.609
5
DWN001 Down Syndrome 70 1.515
6
CHR178 Chromosomal Triplication 34 1.515
7
BTN003 Biotinidase Deficiency 62 1.459
8
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.285
9
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 50 1.258
10
ORG002 Organic Acidemia 43 0.591
11
MTB004 Metabolic Acidosis 48 0.512
12
P ALP008 Alopecia 53 0.418
13
ATS010 Autosomal Recessive Disease 42 0.362
14
BTN004 Biotin Deficiency 44 0.362
15
c INH020 Inherited Metabolic Disorder 47 0.362
16
HYP056 Hypoglycemia 65 0.362
17
P MPL001 Maple Syrup Urine Disease 69 0.295
18
HLC001 Holocarboxylase Synthetase Deficiency 47 0.295
19
P EXN002 Exanthem 58 0.295
20
P RSP003 Respiratory Failure 74 0.295
21
OCL069 Ocular Motor Apraxia 57 0.209
22
c BRN108 Branchiootic Syndrome 1 63 0.209
23
c MCR133 Microvascular Complications of Diabetes 4 41 0.209
24
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.209
25
c ATR087 Atrial Standstill 1 74 0.209
26
SCR003 Secretory Diarrhea 35 0.209
27
c MCR113 Microvascular Complications of Diabetes 3 52 0.209
28
c MCR130 Microvascular Complications of Diabetes 6 41 0.209
29
c MCR120 Microvascular Complications of Diabetes 7 47 0.209
30
CYN002 Cyanosis, Transient Neonatal 43 0.209
31
ENC005 Encephalomalacia 43 0.209
32
P CND004 Candidiasis 57 0.209
33
P DRR001 Diarrhea 55 0.209
34
P LCT001 Lactic Acidosis 50 0.209
35
P CRB088 Cerebral Atrophy 33 0.209
36
P ENC018 Encephalopathy 62 0.209
37
MLT018 Multiple Carboxylase Deficiency 45 0.209
38
P MYP004 Myopathy 67 0.209
39
ALP048 Alopecia Totalis 31 0.209
40
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 0.209
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