Search results for arg1

60 hits were found for arg1

# Family MCID Name MIFTS Score
1
ARG007 Argininemia 57 21.819
2
P HPT023 Hepatocellular Carcinoma 100 3.598
3
AST005 Asthma 76 3.062
4
c ATM011 Autoimmune Hepatitis 63 3.062
5
P MYC007 Myocardial Infarction 70 2.582
6
QDR001 Quadriplegia 48 2.582
7
c HYP595 Hypertension, Essential 84 2.544
8
c DLT002 Dilated Cardiomyopathy 79 2.544
9
LSH001 Leishmaniasis 63 2.500
10
CTN007 Cutaneous Leishmaniasis 62 2.500
11
SPN186 Spinal Cord Injury 60 2.500
12
LNG099 Lung Disease 60 2.500
13
QFV001 Q Fever 60 2.500
14
SCH014 Schistosomiasis 57 2.500
15
INT017 Intestinal Schistosomiasis 48 2.500
16
DRY001 Dry Eye Syndrome 47 2.500
17
P INN002 Inner Ear Disease 47 2.500
18
OBS082 Obstructive Nephropathy 42 2.500
19
c MNT151 Mental Retardation, Autosomal Recessive 18 20 1.870
20
URC002 Urea Cycle Disorder 51 1.826
21
SPS004 Spastic Quadriplegia 39 1.826
22
RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 1.768
23
SPS003 Spastic Diplegia 51 1.768
24
PRS034 Parasitic Helminthiasis Infectious Disease 50 1.768
25
c CRD087 Cardiomyopathy, Familial Hypertrophic, 10 37 1.768
27
c SCH045 Schizophrenia 12 32 1.768
28
GST018 Gastrointestinal Tularemia 27 1.768
29
CRB017 Cerebral Falx Meningioma 26 1.768
30
BRS043 Breast Leiomyosarcoma 26 1.768
31
BRS029 Breast Myoepithelial Carcinoma 25 1.768
32
P STM003 Stomach Carcinoma in Situ 25 1.768
33
ULC005 Ulcer of Lower Limbs 23 1.768
34
HPT005 Hepatic Flexure Cancer 22 1.768
35
MXD042 Mixed Fibrolamellar Hepatocellular Carcinoma 21 1.768
36
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.122
37
SPS019 Spastic Paraparesis 38 0.122
38
P NRB001 Neuroblastoma 72 0.099
39
P PRS040 Prostate Cancer 97 0.070
40
STR067 Stroke, Ischemic 81 0.070
41
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.070
42
c ATR087 Atrial Standstill 1 75 0.070
43
CRB037 Cerebral Palsy 69 0.070
44
MLD001 Melioidosis 68 0.070
45
c HRD010 Hereditary Spastic Paraplegia 66 0.070
46
P DBT009 Diabetes Mellitus 64 0.070
47
CHK001 Chikungunya 57 0.070
48
c ACT075 Acute Myocardial Infarction 57 0.070
49
ALL006 Allergic Asthma 56 0.070
50
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 55 0.070
51
PRP016 Paraplegia 52 0.070
52
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.070
53
ATS010 Autosomal Recessive Disease 48 0.070
54
c INH020 Inherited Metabolic Disorder 47 0.070
55
RSP021 Respiratory Allergy 45 0.070
56
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.070
57
ALL014 Allergic Encephalomyelitis 38 0.070
58
P CRB088 Cerebral Atrophy 37 0.070
59
c KNN009 Kenny-Caffey Syndrome, Type 1 34 0.070
60
ORN004 Ornithinemia 17 0.070
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