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Search results for Luteinizing hormone releasing hormone human acetate salt (LHRH)

107 hits were found for Luteinizing hormone releasing hormone human acetate salt (LHRH)

# Family MCID Name MIFTS Score
1
P PRS040 Prostate Cancer 97 0.821
2
P BRS047 Breast Cancer 97 0.684
3
INS024 Insulin-Like Growth Factor I 79 0.669
4
ADN018 Adenoma 59 0.605
5
P PLY011 Polycystic Ovary Syndrome 56 0.603
6
HYP080 Hypogonadism 50 0.599
7
P INF032 Infertility 57 0.595
8
P HYP086 Hypothyroidism 69 0.591
9
HYP056 Hypoglycemia 66 0.525
10
AMN001 Amenorrhea 54 0.519
11
P ADN016 Adenocarcinoma 64 0.511
12
48X005 48,xyyy 39 0.499
13
P OVR042 Ovarian Cancer 88 0.477
14
ACR007 Acromegaly 71 0.467
15
BNR002 Bone Resorption Disease 48 0.460
16
PRT037 Pertussis 65 0.453
17
CYT002 Cytokine Deficiency 42 0.452
18
P OST002 Osteoporosis 74 0.425
19
P HYP730 Hypogonadotropic Hypogonadism 52 0.416
20
CHL014 Cholera 59 0.405
21
PRS045 Prostatic Hypertrophy 53 0.404
22
P TRN020 Turner Syndrome 67 0.398
23
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.398
24
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.397
25
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.392
26
LMY002 Leiomyoma 52 0.372
27
PRS021 Prostatic Adenoma 51 0.372
28
P PTT006 Pituitary Adenoma 55 0.365
29
PRS129 Prostatic Hyperplasia, Benign 49 0.358
30
HYP020 Hyperprolactinemia 64 0.356
31
ANV001 Anovulation 47 0.340
32
P HRT032 Heart Disease 75 0.336
33
OST159 Osteogenic Sarcoma 66 0.331
34
AGN016 Aging 56 0.321
35
DWN001 Down Syndrome 70 0.321
36
P DRR001 Diarrhea 55 0.319
37
ALL026 Allergic Hypersensitivity Disease 62 0.316
38
P HYP083 Hypopituitarism 53 0.316
39
P HPT023 Hepatocellular Carcinoma 100 0.314
40
AZS001 Azoospermia 50 0.309
41
ANR007 Anorexia Nervosa 63 0.299
42
c RHB024 Rhabdomyosarcoma 2 67 0.298
43
P PNC035 Pancreatic Cancer 84 0.298
44
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.294
45
P CRN300 Coronary Heart Disease 1 63 0.294
46
P CRD246 Cardiovascular System Disease 57 0.290
47
c PCH010 Pachyonychia Congenita 3 44 0.290
48
P ALZ034 Alzheimer Disease 88 0.290
49
c NRF023 Neurofibromatosis, Type Ii 80 0.289
50
PPL052 Papillomatosis, Confluent and Reticulated 33 0.287
51
47X002 47,xyy 49 0.282
52
HYP043 Hyperandrogenism 48 0.281
53
P NTR004 Neutropenia 63 0.280
54
IMP005 Impotence 52 0.280
55
P OVR049 Ovarian Disease 52 0.279
56
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.279
57
RCK004 Rickets 68 0.276
58
TTN003 Tetanus 65 0.273
59
P OVR046 Ovarian Cyst 47 0.262
60
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.258
61
P MLN007 Male Infertility 55 0.257
62
P MLN008 Melanoma 69 0.250
63
CYS001 Cystic Fibrosis 81 0.247
64
P LYM118 Lymphoma 68 0.247
65
DRM006 Dermatitis 61 0.246
66
URM002 Uremia 49 0.243
67
P DBT005 Diabetes Insipidus 55 0.243
68
LPP008 Lipoprotein Quantitative Trait Locus 62 0.243
69
END062 Endometrial Hyperplasia 48 0.237
70
OVR094 Ovarian Epithelial Cancer 38 0.235
71
NTR005 Nutritional Deficiency Disease 62 0.234
72
P BLD134 Bladder Cancer 79 0.232
73
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.231
74
SPN186 Spinal Cord Injury 60 0.227
75
ATX019 Ataxia with Vitamin E Deficiency 42 0.222
76
P MYC007 Myocardial Infarction 70 0.218
77
SPP011 Suppression of Tumorigenicity 12 59 0.216
78
PTT009 Pituitary Gland Disease 54 0.212
79
ART140 Arteries, Anomalies of 52 0.207
80
P HDC001 Headache 57 0.199
81
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.198
82
OLG001 Oligospermia 45 0.187
83
P ALC033 Alcohol Use Disorder 58 0.185
84
P SKN015 Skin Carcinoma 66 0.183
85
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.182
86
c PLY105 Polycystic Ovary Syndrome 1 38 0.182
87
DPH001 Diphtheria 60 0.181
88
PRM020 Premenstrual Tension 40 0.169
89
P KDN017 Kidney Cancer 60 0.168
90
ETN001 Eating Disorder 60 0.167
91
ARG004 Argyria 27 0.167
92
P PRP029 Porphyria 62 0.161
93
BRS051 Breast Disease 58 0.159
94
P CNR004 Cone-Rod Dystrophy 2 73 0.158
95
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.158
96
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.152
97
P HYD006 Hydrocephalus 66 0.150
98
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.147
99
FCT007 Factor Vii Deficiency 67 0.146
100
PRP030 Purpura 54 0.145
101
PNC129 Pancreatic Adenocarcinoma 68 0.145
102
HYD002 Hydronephrosis 60 0.129
103
TRN018 Transitional Cell Carcinoma 56 0.127
104
c HMC039 Hemochromatosis, Type 1 74 0.122
105
49X006 49, Xxxxy Syndrome 41 0.112
106
BLM002 Bulimia Nervosa 57 0.107
107
MRG013 Mirage Syndrome 43 0.065
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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