Search results for hamp

202 hits were found for hamp

# Family MCID Name MIFTS Score
1
c HMC019 Hemochromatosis, Type 2b 35 38.538
2
c HMC039 Hemochromatosis, Type 1 73 36.806
3
c HMC009 Hemochromatosis Type 2 58 31.823
4
DFC004 Deficiency Anemia 74 15.504
5
P PRP003 Porphyria Cutanea Tarda 66 12.815
6
HMS001 Hemosiderosis 48 11.862
7
P RRH023 Rare Hereditary Hemochromatosis 53 11.858
8
IRN001 Iron Deficiency Anemia 58 11.363
9
MLR004 Malaria 78 11.325
10
c SYS001 Systemic Lupus Erythematosus 86 11.325
11
IRN002 Iron Metabolism Disease 56 10.352
12
P PRP029 Porphyria 60 10.328
13
c BTT014 Beta-Thalassemia 72 9.873
14
P ART023 Arthropathy 60 9.690
15
EXT033 Extrapulmonary Tuberculosis 45 9.617
16
c CHR684 Chronic Kidney Disease 74 9.590
17
P SDR003 Sideroblastic Anemia 49 9.560
18
P PLY018 Polycythemia 56 9.489
19
MYL009 Myelodysplastic Syndrome 67 9.445
20
c ANM036 Anemia, Sideroblastic, 1 56 9.445
21
ALP103 Alpha-1-Antitrypsin Deficiency 67 9.387
22
HMG005 Hemoglobinopathy 55 9.387
23
P CNG003 Congenital Dyserythropoietic Anemia 48 9.387
24
c TYP009 Type 2 Diabetes Mellitus 92 9.247
25
PLY001 Polycythemia Vera 69 9.247
26
P RST001 Restless Legs Syndrome 52 9.247
27
c HMC021 Hemochromatosis, Type 2a 41 8.579
28
MCR018 Microcytic Anemia 47 7.133
29
c HMC035 Hemochromatosis, Type 4 52 7.099
30
P SDR002 Siderosis 42 7.003
31
ACR006 Aceruloplasminemia 63 6.909
32
ATR002 Atransferrinemia 50 6.818
33
HYP801 Hyperferritinemia with or Without Cataract 53 6.736
34
HYP001 Hypochromic Microcytic Anemia 36 6.736
35
c HMC010 Hemochromatosis, Type 3 49 6.678
36
CTN011 Cutaneous Porphyria 44 6.678
37
c ALP101 Alpha-Thalassemia 62 6.678
38
P ERY048 Erythrocytosis, Familial, 2 56 6.538
39
IRN008 Iron Overload in Africa 51 6.538
40
c ANM049 Anemia, Congenital Dyserythropoietic, Type Ib 39 6.538
41
MNR003 Mineral Metabolism Disease 35 6.538
42
c ANM043 Anemia, Congenital Dyserythropoietic, Type Ia 52 6.538
43
P HMG032 Hemoglobin H Disease 51 6.538
44
ANM001 Anemia of Prematurity 30 6.538
45
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 6.538
46
MLT113 Multicentric Castleman Disease 47 6.538
47
c ACQ010 Acquired Polycythemia 46 6.538
48
c INH020 Inherited Metabolic Disorder 47 6.538
49
c CNG027 Congenital Hemolytic Anemia 49 6.538
50
NTR005 Nutritional Deficiency Disease 60 6.538
51
FLC001 Folic Acid Deficiency Anemia 28 6.538
52
MTL002 Metal Metabolism Disorder 30 6.538
53
c LNG001 Lung Clear Cell Carcinoma 29 6.538
54
HLX001 Helix Syndrome 47 5.319
55
FTT001 Fatty Liver Disease 61 1.945
56
P HPT023 Hepatocellular Carcinoma 95 1.891
57
THY116 Thyroid Carcinoma, Nonmedullary, with or Without Cell Oxyphilia 17 1.425
58
c HPT001 Hepatitis C 61 1.368
59
KWS002 Kawasaki Disease 65 1.348
60
P VSC011 Vasculitis 61 1.348
61
BCT022 Bacterial Infectious Disease 56 1.337
62
c HPT073 Hepatitis C Virus 71 1.321
63
ATS010 Autosomal Recessive Disease 42 1.271
64
P HPT021 Hepatitis 68 1.271
65
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.235
66
HYP080 Hypogonadism 49 1.216
67
P LNG032 Lung Cancer 98 1.107
68
HYP266 Hypoxia 56 1.107
69
P THL005 Thalassemia 56 1.085
70
P ALZ034 Alzheimer Disease 87 1.081
71
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.081
72
TRN072 Transferrin Serum Level Quantitative Trait Locus 2 17 1.054
73
P HYP730 Hypogonadotropic Hypogonadism 54 1.054
74
P MCR129 Microvascular Complications of Diabetes 1 68 1.054
75
c MCR120 Microvascular Complications of Diabetes 7 47 1.054
76
VRG001 Variegate Porphyria 55 1.054
77
c SML038 Small Cell Cancer of the Lung 69 1.024
78
PPL052 Papillomatosis, Confluent and Reticulated 34 0.991
79
c DWL002 Dowling-Degos Disease 1 58 0.953
80
AMN001 Amenorrhea 53 0.953
81
HYP066 Hyperglycemia 60 0.953
82
P CRN074 Coronary Artery Aneurysm 41 0.953
83
c ATS007 Autism Spectrum Disorder 72 0.909
84
P SLP005 Sleep Disorder 62 0.909
85
P BRS047 Breast Cancer 97 0.602
86
P PNC035 Pancreatic Cancer 86 0.602
88
SPL018 Splenomegaly 47 0.560
89
P HDC001 Headache 56 0.485
90
P PRD008 Periodontitis 64 0.485
91
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.464
92
P HML002 Hemolytic Anemia 62 0.464
93
KRT002 Keratomalacia 54 0.443
94
THL010 Thalassemia Minor 31 0.420
95
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.420
96
ATH013 Atherosclerosis Susceptibility 63 0.396
97
BTT017 Beta-Thalassemia Major 53 0.396
98
P MYC084 Mycobacterium Tuberculosis 1 68 0.371
99
P SCK005 Sickle Cell Disease 56 0.371
100
GLC003 Glucose Intolerance 53 0.343
101
IRN004 Iron-Refractory Iron Deficiency Anemia 46 0.343
102
P BND020 Bone Disease 60 0.343
103
LVR012 Liver Cirrhosis 62 0.343
104
URM002 Uremia 47 0.343
105
P LVR013 Liver Disease 68 0.343
106
P KDN018 Kidney Disease 72 0.343
107
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.313
108
TYP007 Typhoid Fever 63 0.313
109
BLR008 Bilirubin Metabolic Disorder 57 0.313
110
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 48 0.280
111
c CHL119 Cholangitis, Primary Sclerosing 57 0.280
112
CHL067 Cholecystitis 59 0.280
113
P SCL009 Sclerosing Cholangitis 46 0.280
114
P CHL066 Cholangitis 51 0.280
115
HRD218 Hereditary Stomatocytosis 31 0.280
116
MYL069 Myeloma, Multiple 77 0.243
117
NNL006 Non-Alcoholic Steatohepatitis 54 0.243
118
IMP005 Impotence 52 0.243
119
CYT002 Cytokine Deficiency 43 0.243
120
PRT036 Peritonitis 65 0.243
121
AGN016 Aging 54 0.198
122
P GST053 Gastric Cancer 82 0.198
123
RCK004 Rickets 65 0.198
124
c ATR087 Atrial Standstill 1 74 0.198
125
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.198
126
c VRL010 Viral Hepatitis 52 0.198
127
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.198
128
MST005 Mastitis 52 0.198
129
SLC006 Silicosis 55 0.198
130
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.198
131
P BCL017 B-Cell Lymphoma 57 0.198
132
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.140
133
HLC007 Helicobacter Pylori Infection 67 0.140
134
c PRD040 Periodontitis, Chronic 52 0.140
135
P LKM062 Leukemia, Acute Lymphoblastic 69 0.140
136
c GLL025 Gallbladder Disease 2 12 0.140
137
ACT119 Acute Promyelocytic Leukemia 62 0.140
138
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.140
140
MLD018 Mild Cognitive Impairment 48 0.140
141
P SNS001 Sensorineural Hearing Loss 59 0.140
142
PRT013 Portal Hypertension 59 0.140
143
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.140
144
P END033 Endocarditis 58 0.140
145
P MDL005 Medulloblastoma 75 0.140
146
ALC007 Alcohol Dependence 65 0.140
147
BRK010 Burkitt Lymphoma 66 0.140
148
c FNC027 Fanconi Anemia, Complementation Group a 81 0.140
149
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.140
150
P FRD001 Friedreich Ataxia 62 0.140
151
P FML018 Familial Mediterranean Fever 73 0.140
152
INF034 Infective Endocarditis 53 0.140
153
INT029 Interleukin-7 Receptor Alpha Deficiency 28 0.140
154
P FML011 Familial Adenomatous Polyposis 71 0.140
155
P APL001 Aplastic Anemia 73 0.140
156
SCK003 Sickle Cell Anemia 74 0.140
157
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.140
158
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.140
159
HRN029 Hearing Loss, Noise-Induced 37 0.140
160
HMX003 Heme Oxygenase 1 Deficiency 26 0.140
161
LPT014 Leptin Deficiency or Dysfunction 77 0.140
162
HPT004 Hepatic Coma 43 0.140
163
P GLM040 Glioma Susceptibility 1 70 0.140
164
BRC012 Brucellosis 66 0.140
165
P ALC033 Alcohol Use Disorder 67 0.140
166
MSC190 Muscular Disease 36 0.140
167
BTT018 Beta-Thalassemia Intermedia 31 0.140
168
CLT003 Colitis 63 0.140
169
CHL068 Cholestasis 61 0.140
170
MLG169 Malignant Astrocytoma 57 0.140
171
ISC004 Ischemia 61 0.140
172
CNT047 Contact Dermatitis 57 0.140
173
P CNJ013 Conjunctivitis 66 0.140
174
P DYS154 Dystonia 64 0.140
175
PRT037 Pertussis 49 0.140
176
c ATM011 Autoimmune Hepatitis 62 0.140
177
P CRD246 Cardiovascular System Disease 55 0.140
178
BRN028 Brain Cancer 73 0.140
179
HPT019 Hepatic Encephalopathy 59 0.140
180
P HYP086 Hypothyroidism 69 0.140
181
TXC005 Toxic Shock Syndrome 62 0.140
182
ALC006 Alcoholic Hepatitis 61 0.140
183
LYM017 Lyme Disease 63 0.140
184
P HRT032 Heart Disease 84 0.140
185
P LKM002 Leukemia 66 0.140
186
IRR003 Irritant Dermatitis 47 0.140
187
P RHN004 Rhinitis 57 0.140
188
THR004 Thrombocytosis 52 0.140
189
P ART021 Arteriosclerosis 53 0.140
190
GRC001 Gracile Syndrome 47 0.140
191
SDD008 Sudden Sensorineural Hearing Loss 41 0.140
192
OCC001 Occupational Dermatitis 27 0.140
193
DRM006 Dermatitis 62 0.140
194
P ENC018 Encephalopathy 62 0.140
195
CRH001 Crohn's Disease 80 0.140
196
VSC002 Vascular Dementia 59 0.140
197
48X005 48,xyyy 39 0.140
198
c CNT101 Central Congenital Hypothyroidism 37 0.140
199
ULC004 Ulcerative Colitis 74 0.140
200
CHL061 Childhood Leukemia 47 0.140
201
P DBT009 Diabetes Mellitus 67 0.140
202
MCR004 Macroglobulinemia 48 0.140
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