Search results for acid-labile subunit

66 hits were found for acid-labile subunit

# Family MCID Name MIFTS Score
1
ACD008 Acid-Labile Subunit Deficiency 46 16.123
2
c BLD140 Blood Group, I System 37 0.420
3
ACR007 Acromegaly 70 0.214
4
INS024 Insulin-Like Growth Factor I 83 0.209
5
PRS047 Prostatitis 59 0.158
6
P PRS040 Prostate Cancer 88 0.151
7
END072 Endotheliitis 46 0.150
8
P HPT021 Hepatitis 75 0.141
9
AGN016 Aging 65 0.138
10
P DBT009 Diabetes Mellitus 72 0.136
11
GRW007 Growth Hormone Deficiency 52 0.126
12
P CLR023 Colorectal Cancer 98 0.123
13
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.119
14
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.119
15
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.119
16
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.119
17
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.119
18
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.119
19
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.119
20
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.119
21
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.119
22
P HYP086 Hypothyroidism 62 0.117
23
SND001 Sandhoff Disease 65 0.106
24
LRN002 Laron Syndrome 63 0.103
25
P HYP083 Hypopituitarism 59 0.103
26
MMM006 Mammographic Density 43 0.103
27
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.102
28
c HPT001 Hepatitis C 73 0.100
29
c HPT073 Hepatitis C Virus 73 0.098
30
P HRT032 Heart Disease 80 0.086
31
P LPS004 Lupus Erythematosus 69 0.086
32
P ANR048 Aniridia 1 68 0.086
33
c SYS001 Systemic Lupus Erythematosus 86 0.083
34
SHW002 Shwachman-Diamond Syndrome 63 0.083
35
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 53 0.083
36
ANR038 Anorexia Nervosa 1 21 0.083
37
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.083
38
BLD137 Blood Group--Ahonen 17 0.083
39
MLT157 Multiple System Atrophy 1 65 0.078
40
HYP056 Hypoglycemia 62 0.078
41
P STS008 Sotos Syndrome 1 56 0.078
42
c CNT075 Central Precocious Puberty 52 0.078
43
P PRC019 Precocious Puberty 52 0.078
44
P TRN020 Turner Syndrome 69 0.073
45
P CRN300 Coronary Heart Disease 1 57 0.073
46
P SLV001 Silver-Russell Syndrome 57 0.073
47
BRN106 Burns 57 0.073
48
ISL001 Islet Cell Tumor 54 0.073
49
c OST164 Osteoporosis, Juvenile 54 0.073
50
c BLM008 Bulimia Nervosa 2 53 0.073
51
OST016 Osteochondrosis 52 0.073
52
CMP034 Complete Androgen Insensitivity Syndrome 47 0.073
53
c PTT056 Pituitary Adenoma 1, Multiple Types 46 0.073
54
FTL021 Fetal Macrosomia 46 0.073
55
ISL015 Isolated Growth Hormone Deficiency, Type Ib 44 0.073
56
HYP070 Hyperpituitarism 43 0.073
57
P SLL003 Salla Disease 43 0.073
58
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 42 0.073
59
c SCN052 Secondary Adrenal Insufficiency 41 0.073
60
MNN006 Meninges Hemangiopericytoma 39 0.073
61
PSD008 Pseudopapilledema 37 0.073
62
SLP010 Slipped Capital Femoral Epiphysis 37 0.073
63
FST010 Fasting Hypoglycemia 36 0.073
64
OCL004 Ocular Hyperemia 31 0.073
65
ALR002 Al-Raqad Syndrome 30 0.073
66
GRW003 Growth Hormone Insensitivity with Immunodeficiency 21 0.073
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