Search results for hk1

215 hits were found for hk1

# Family MCID Name MIFTS Score
1
NRP010 Neuropathy, Hereditary Motor and Sensory, Russe Type 36 37.793
2
NRD073 Neurodevelopmental Disorder with Visual Defects and Brain Anomalies 22 36.280
3
HML052 Hemolytic Anemia, Nonspherocytic, Due to Hexokinase Deficiency 26 34.684
4
c RTN195 Retinitis Pigmentosa 79 22 32.288
5
P RTN008 Retinitis Pigmentosa 79 21.328
6
FND002 Fundus Dystrophy 55 20.408
7
P HML002 Hemolytic Anemia 62 18.947
8
P NRP001 Neuropathy 59 15.775
9
P DBT009 Diabetes Mellitus 67 13.737
10
P CNR004 Cone-Rod Dystrophy 2 75 13.261
11
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 58 11.927
12
P CHR071 Charcot-Marie-Tooth Disease 64 11.927
13
ATS010 Autosomal Recessive Disease 42 11.216
14
c AMY091 Amyotrophic Lateral Sclerosis 1 88 11.155
15
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 9.226
16
c HYP349 Hyperinsulinemic Hypoglycemia, Familial, 7 43 7.694
17
P NSP012 Nasopharyngeal Carcinoma 60 3.430
18
NRR001 Neuroretinitis 42 2.591
19
RTN023 Retinitis 45 2.591
20
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 1.859
21
P SZR006 Seizure Disorder 69 1.532
22
P GST053 Gastric Cancer 82 1.459
23
P RTN016 Retinal Degeneration 52 1.459
24
P CLR023 Colorectal Cancer 100 1.395
25
PPL022 Papilloma 53 1.361
26
c INH030 Inherited Retinal Disorder 28 1.340
27
MYL069 Myeloma, Multiple 77 1.338
28
SQM002 Squamous Cell Papilloma 45 1.291
29
SNS003 Sensory Peripheral Neuropathy 51 1.185
30
ADN011 Adenoid Cystic Carcinoma 68 1.167
31
P SLV026 Salivary Gland Carcinoma 60 1.167
32
MYP002 Myoepithelial Carcinoma 46 1.167
33
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.167
34
CRV013 Cervical Adenoid Cystic Carcinoma 33 1.167
35
MCP006 Mucoepidermoid Carcinoma 48 1.167
36
ORL011 Oral Cancer 60 1.167
37
P MLN008 Melanoma 75 1.143
38
HYP056 Hypoglycemia 65 1.143
39
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 1.098
40
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 1.098
41
HYP060 Hyperinsulinism 53 1.098
42
KRT009 Keratosis 52 1.068
43
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.046
44
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.046
45
PRT037 Pertussis 49 1.046
46
c CHR516 Charcot-Marie-Tooth Disease, Type 4c 48 1.017
47
TTH006 Tooth Disease 51 1.017
48
c CHR376 Charcot-Marie-Tooth Disease, Type 4d 48 1.017
49
P NGH001 Night Blindness 52 1.017
50
CHR178 Chromosomal Triplication 34 1.017
51
CHR182 Chromosome 10p Duplication 25 1.017
52
P AST005 Asthma 76 0.948
53
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 33 0.948
54
P ANR048 Aniridia 1 66 0.948
55
NRL016 Neural Tube Defects 81 0.948
56
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.948
57
P RTN018 Retinal Disease 53 0.948
58
MYL020 Myelomeningocele 51 0.847
59
P PNC035 Pancreatic Cancer 86 0.795
60
PRM236 Primary Biliary Cholangitis 62 0.698
61
P OVR042 Ovarian Cancer 88 0.642
62
P BRS047 Breast Cancer 97 0.602
63
P CHL066 Cholangitis 51 0.596
64
HYP266 Hypoxia 56 0.547
65
GST019 Gastrointestinal Stromal Tumor 78 0.530
66
P SCH015 Schizophrenia 74 0.474
67
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.474
68
LYM017 Lyme Disease 63 0.474
69
P SKN015 Skin Carcinoma 71 0.474
70
HYP066 Hyperglycemia 60 0.474
71
ART140 Arteries, Anomalies of 52 0.433
72
AGN016 Aging 54 0.433
73
LPP008 Lipoprotein Quantitative Trait Locus 65 0.433
74
c MJR024 Major Affective Disorder 9 40 0.433
75
c MJR022 Major Affective Disorder 8 37 0.433
76
GLB002 Glioblastoma 67 0.433
77
P BPL003 Bipolar Disorder 56 0.433
78
PSY004 Psychotic Disorder 66 0.433
79
P RTN024 Retinoblastoma 72 0.410
80
P HPT023 Hepatocellular Carcinoma 95 0.387
81
SKN013 Skin Benign Neoplasm 49 0.387
82
P ALP008 Alopecia 53 0.387
83
P SPP010 Suppressor of Tumorigenicity 3 51 0.362
84
P PLM037 Pulmonary Hypertension 69 0.362
85
c TYP008 Type 1 Diabetes Mellitus 77 0.362
86
ORL015 Oral Squamous Cell Carcinoma 43 0.362
87
P ADN016 Adenocarcinoma 63 0.362
88
LVR012 Liver Cirrhosis 62 0.362
89
END040 Endogenous Depression 54 0.362
90
GST033 Gestational Diabetes 61 0.362
91
P ALZ034 Alzheimer Disease 87 0.335
92
P LNG032 Lung Cancer 98 0.335
93
SQM006 Squamous Cell Carcinoma 59 0.335
94
ADR016 Adrenal Cortical Carcinoma 61 0.306
95
ADR041 Adrenal Cortical Adenoma 48 0.306
96
DFF010 Diffuse Alopecia Areata 23 0.306
97
c MST023 Mesothelioma, Malignant 56 0.306
98
DFC004 Deficiency Anemia 74 0.306
99
P KDN017 Kidney Cancer 60 0.306
100
SKN016 Skin Disease 62 0.306
101
P BNG032 Benign Mesothelioma 53 0.306
102
SYS003 Systolic Heart Failure 49 0.306
103
P BLD134 Bladder Cancer 79 0.274
104
P INF037 Inflammatory Bowel Disease 53 0.274
105
P EPL164 Epilepsy 70 0.274
106
P LTR001 Lateral Sclerosis 58 0.274
107
P TMP001 Temporal Lobe Epilepsy 49 0.274
108
GLC105 Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency 33 0.237
109
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.237
110
P RHM011 Rheumatoid Arthritis 81 0.237
111
MTG002 Mutagen Sensitivity 35 0.237
112
c SML038 Small Cell Cancer of the Lung 69 0.237
113
P LNG064 Lung Cancer Susceptibility 3 70 0.237
114
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.237
115
c BSL007 Basal Cell Carcinoma 68 0.237
116
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.237
117
GLM045 Glioma 62 0.237
118
GLL048 Glial Tumor 52 0.237
119
c HRD088 Hereditary Neuropathies 34 0.237
120
P ART022 Arthritis 70 0.237
121
P BCL017 B-Cell Lymphoma 57 0.237
122
c TYP009 Type 2 Diabetes Mellitus 92 0.193
123
ERY029 Erythermalgia, Primary 58 0.193
124
ANX010 Anxiety 70 0.193
125
P LKM062 Leukemia, Acute Lymphoblastic 69 0.193
126
P PRK039 Parkinsonism 55 0.193
127
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 63 0.193
128
P SPN408 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1 52 0.193
129
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.193
130
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.193
131
EPD002 Epidermolytic Hyperkeratosis 55 0.193
132
PMP004 Pemphigus Foliaceus 43 0.193
133
P HRD021 Hereditary Sensory Neuropathy 48 0.193
134
ACT098 Acute Erythroid Leukemia 55 0.193
135
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.193
136
CNG034 Congestive Heart Failure 69 0.193
137
ASP004 Asphyxia Neonatorum 50 0.193
138
P ADL010 Adult Respiratory Distress Syndrome 71 0.193
139
INS001 Insulinoma 59 0.193
140
P KRT005 Keratoacanthoma 47 0.193
141
PRP030 Purpura 54 0.193
142
P INS002 in Situ Carcinoma 53 0.193
143
LNG016 Lung Papillary Adenocarcinoma 20 0.193
144
AMY005 Amyloid Neuropathy 31 0.193
146
P PMP001 Pemphigus 55 0.193
147
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 36 0.193
148
P RNG032 Ring Chromosome 39 0.193
149
PRM329 Premature Aging 36 0.193
150
THY029 Thyroid Carcinoma 54 0.193
151
P PRS040 Prostate Cancer 95 0.137
152
c CHR517 Charcot-Marie-Tooth Disease, Type 4a 45 0.137
153
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.137
154
HLX001 Helix Syndrome 47 0.137
155
DFF005 Diffuse Large B-Cell Lymphoma 55 0.137
156
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.137
157
DSS032 Disease by Infectious Agent 55 0.137
158
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.137
159
P PLY014 Polycystic Kidney Disease 71 0.137
160
NNL006 Non-Alcoholic Steatohepatitis 54 0.137
161
PRX015 Paroxysmal Extreme Pain Disorder 56 0.137
162
PLN006 Poland Syndrome 45 0.137
163
ACN002 Acanthosis Nigricans 56 0.137
164
RTN017 Retinal Detachment 60 0.137
165
CLR109 Colorectal Adenocarcinoma 50 0.137
166
P DRM053 Dermatitis, Atopic 65 0.137
167
c CHR519 Charcot-Marie-Tooth Disease, Type 4b2 48 0.137
168
c CHR420 Charcot-Marie-Tooth Disease, Type 4j 48 0.137
169
c EXS020 Exostoses, Multiple, Type Ii 38 0.137
170
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.137
171
c CHR504 Charcot-Marie-Tooth Disease, Type 4b3 45 0.137
172
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.137
173
P FRG001 Fragile X Syndrome 70 0.137
174
c CHR521 Charcot-Marie-Tooth Disease, Type 4b1 47 0.137
175
ANN002 Anencephaly 57 0.137
176
c CHR421 Charcot-Marie-Tooth Disease, Type 4h 46 0.137
177
c CHR670 Charcot-Marie-Tooth Disease, Demyelinating, Type 4f 43 0.137
178
P LKM071 Leukemia, Chronic Lymphocytic 74 0.137
179
c CNG012 Congenital Generalized Lipodystrophy 65 0.137
180
P PLY019 Polyneuropathy 53 0.137
181
ISC004 Ischemia 61 0.137
182
P CYS039 Cystic Kidney Disease 52 0.137
183
P INF032 Infertility 60 0.137
184
P PRP019 Peripheral Nervous System Disease 57 0.137
185
IRN002 Iron Metabolism Disease 56 0.137
186
P LRY044 Larynx Cancer 53 0.137
187
P ECL001 Eclampsia 52 0.137
188
P MLN007 Male Infertility 56 0.137
189
FLR002 Filariasis 55 0.137
190
P HRT032 Heart Disease 84 0.137
191
TTN003 Tetanus 64 0.137
192
P LKM002 Leukemia 66 0.137
193
P LRY019 Laryngitis 53 0.137
194
CLN015 Colon Adenocarcinoma 64 0.137
195
P FBR017 Fibrosarcoma 55 0.137
196
THL004 Theileriasis 26 0.137
197
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.137
198
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 0.137
199
c RNG005 Ring Chromosome 10 26 0.137
200
P HYP265 Hypotonia 42 0.137
201
P KDN018 Kidney Disease 72 0.137
202
SPL018 Splenomegaly 47 0.137
203
FTD001 Foot Drop 36 0.137
204
CHR176 Chromophil Renal Cell Carcinoma 23 0.137
205
TRM010 Traumatic Brain Injury 50 0.137
206
P PSR002 Psoriasis 63 0.137
207
P HYP076 Hyperthyroidism 53 0.137
208
BRR012 Berardinelli-Seip Congenital Lipodystrophy 26 0.137
209
47X002 47,xyy 48 0.137
210
FTT001 Fatty Liver Disease 61 0.137
211
P ENC008 Encephalocele 46 0.137
212
MNN020 Meningococcal Infection 45 0.137
213
PRT187 Partial Duplication of Chromosome X 9 0.137
214
c ATS452 Autosomal Recessive Axonal Hereditary Motor and Sensory Neuropathy 18 0.137
215
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.137
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