Search results for Tretinoin

452 hits were found for Tretinoin

# Family MCID Name MIFTS Score
1
P NRF023 Neurofibromatosis, Type Ii 76 0.519
2
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.428
3
c DWL002 Dowling-Degos Disease 1 58 0.245
4
c FNC043 Fanconi Anemia, Complementation Group E 62 0.205
5
ACT119 Acute Promyelocytic Leukemia 63 0.191
6
P LKM002 Leukemia 66 0.174
7
c LKM061 Leukemia, Acute Myeloid 83 0.150
8
P MYL006 Myeloid Leukemia 60 0.150
9
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.150
10
LNT004 Lentigines 46 0.140
11
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.133
12
KRT009 Keratosis 53 0.129
13
c RHB024 Rhabdomyosarcoma 2 65 0.125
14
MYL009 Myelodysplastic Syndrome 70 0.109
15
P SKN015 Skin Carcinoma 67 0.109
16
c BSL007 Basal Cell Carcinoma 68 0.104
17
SKN016 Skin Disease 63 0.104
18
48X005 48,xyyy 39 0.104
19
ADL002 Adult Syndrome 69 0.099
20
RSC001 Rosacea 55 0.099
21
SKN005 Skin Atrophy 43 0.099
22
c CHR064 Chronic Monocytic Leukemia 34 0.099
23
P ALP008 Alopecia 56 0.094
24
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.089
25
P TRN020 Turner Syndrome 65 0.089
26
P LCH002 Lichen Planus 54 0.089
27
P ACT008 Actinic Keratosis 52 0.089
28
MLN073 Melanosis, Neurocutaneous 45 0.089
29
ACN002 Acanthosis Nigricans 60 0.083
30
c ACT073 Acute Leukemia 58 0.083
31
AGN016 Aging 56 0.083
32
KRT013 Keratolytic Winter Erythema 46 0.083
33
P LNG032 Lung Cancer 97 0.077
34
c LKM063 Leukemia, Chronic Myeloid 71 0.077
35
DWN001 Down Syndrome 70 0.077
36
MGK001 Megakaryocytic Leukemia 64 0.077
37
P PSR002 Psoriasis 62 0.077
38
DRM006 Dermatitis 61 0.077
39
ERY051 Erythroleukemia, Familial 56 0.077
40
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 55 0.077
41
c LKM070 Leukemia, Acute Monocytic 53 0.077
42
PST011 Pustulosis of Palm and Sole 52 0.077
43
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.070
44
LYM133 Lymphoma, Hodgkin, Classic 69 0.070
45
MLN008 Melanoma 69 0.070
46
P LYM118 Lymphoma 68 0.070
47
SQM006 Squamous Cell Carcinoma 60 0.070
48
CNT047 Contact Dermatitis 57 0.070
49
KRT002 Keratomalacia 48 0.070
50
IRR003 Irritant Dermatitis 47 0.070
51
LYM019 Lymphosarcoma 47 0.070
52
AND014 Androgenic Alopecia 44 0.070
53
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.063
54
P BLD134 Bladder Cancer 78 0.063
55
DFC004 Deficiency Anemia 75 0.063
56
P CNR004 Cone-Rod Dystrophy 2 71 0.063
57
MYL031 Myeloproliferative Neoplasm 65 0.063
58
P MTR014 Motor Neuron Disease 64 0.063
59
INT002 Intermittent Claudication 61 0.063
60
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.063
61
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.063
62
P CHR285 Chronic Myelomonocytic Leukemia 59 0.063
63
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.063
64
CMR002 Coumarin Resistance 56 0.063
65
ACT200 Acute Monoblastic Leukemia 55 0.063
66
PPL022 Papilloma 54 0.063
67
P ICH004 Ichthyosis 54 0.063
68
P MNC007 Monocytic Leukemia 54 0.063
69
P LTR001 Lateral Sclerosis 53 0.063
70
DYS002 Dysplastic Nevus Syndrome 53 0.063
71
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.063
72
HYP781 Hypoascorbemia 50 0.063
73
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.063
74
ATY042 Atypical Chronic Myeloid Leukemia 49 0.063
75
RFR010 Refractory Anemia 48 0.063
76
ACT098 Acute Erythroid Leukemia 48 0.063
77
ORL013 Oral Lichen Planus 45 0.063
78
IMM064 Immunodeficiency, Common Variable, 10 44 0.063
79
BNM001 Bone Marrow Cancer 43 0.063
80
HYP457 Hypertrophic Scars 43 0.063
81
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.063
82
LCH016 Lichen Sclerosus Et Atrophicus 41 0.063
83
LKP003 Leukoplakia 39 0.063
84
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.063
85
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.063
86
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.063
87
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.063
88
c ADL093 Adult Acute Monocytic Leukemia 20 0.063
89
P OST002 Osteoporosis 73 0.054
90
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.054
91
P NRB001 Neuroblastoma 71 0.054
92
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.054
93
SKN019 Skin Melanoma 67 0.054
94
FCT007 Factor Vii Deficiency 66 0.054
95
MYC006 Mycosis Fungoides 66 0.054
96
c SML038 Small Cell Cancer of the Lung 65 0.054
97
c MLN065 Melanocytic Nevus Syndrome, Congenital 63 0.054
98
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 62 0.054
99
HMT002 Hematologic Cancer 62 0.054
100
SZR001 Sezary's Disease 60 0.054
101
INT303 Intracranial Hypertension, Idiopathic 56 0.054
102
TLN003 Telangiectasis 51 0.054
103
LNG031 Lung Benign Neoplasm 50 0.054
104
KRT001 Keratoconjunctivitis Sicca 50 0.054
105
P ALP061 Alopecia, Androgenetic, 1 49 0.054
106
SKN013 Skin Benign Neoplasm 49 0.054
107
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.054
108
c BSL024 Basal Cell Carcinoma 1 47 0.054
109
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.054
110
49X006 49, Xxxxy Syndrome 41 0.054
111
KLD004 Keloid Disorder 40 0.054
112
ORL012 Oral Leukoplakia 39 0.054
113
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 38 0.054
114
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 35 0.054
115
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.054
116
PHT004 Photoallergic Dermatitis 28 0.054
117
P CLR023 Colorectal Cancer 98 0.044
118
MYL069 Myeloma, Multiple 85 0.044
119
P LNG064 Lung Cancer Susceptibility 3 77 0.044
120
CRV035 Cervical Cancer 76 0.044
121
KPS004 Kaposi Sarcoma 75 0.044
122
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.044
123
P GRF003 Graft-Versus-Host Disease 71 0.044
124
HMN044 Human Immunodeficiency Virus Type 1 71 0.044
125
P SRC025 Sarcoidosis 1 70 0.044
126
ADN011 Adenoid Cystic Carcinoma 70 0.044
127
P LKM062 Leukemia, Acute Lymphoblastic 68 0.044
128
NVS017 Nevus, Epidermal 68 0.044
129
BRK010 Burkitt Lymphoma 67 0.044
130
MNT001 Mantle Cell Lymphoma 66 0.044
131
P FLL037 Follicular Lymphoma 66 0.044
132
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.044
133
SRC014 Sarcoma 65 0.044
134
P ADN016 Adenocarcinoma 64 0.044
135
P NTR004 Neutropenia 63 0.044
136
P KDN017 Kidney Cancer 61 0.044
137
P ALP009 Alopecia Areata 60 0.044
138
CHN016 Cohen Syndrome 57 0.044
139
P EXN002 Exanthem 57 0.044
140
c CHR417 Chronic Graft Versus Host Disease 56 0.044
141
P MYS005 Myositis 56 0.044
142
ALL010 Allergic Contact Dermatitis 55 0.044
143
P LYM031 Lymphocytic Leukemia 55 0.044
144
LYM040 Lymphoblastic Lymphoma 54 0.044
145
P PRK001 Porokeratosis 53 0.044
146
NTR018 Neutrophilia, Hereditary 52 0.044
147
PLS009 Plasma Cell Neoplasm 51 0.044
148
SPN035 Spindle Cell Sarcoma 51 0.044
149
MLL001 Molluscum Contagiosum 49 0.044
150
47X002 47,xyy 49 0.044
151
c FLL041 Follicular Lymphoma 1 49 0.044
152
P HYP058 Hypervitaminosis a 49 0.044
153
ATX019 Ataxia with Vitamin E Deficiency 48 0.044
154
PLS025 Plasmablastic Lymphoma 47 0.044
155
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 46 0.044
156
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.044
157
c PRM038 Primary Agammaglobulinemia 43 0.044
158
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.044
159
SQM002 Squamous Cell Papilloma 42 0.044
160
ANG049 Angioedema Induced by Ace Inhibitors 40 0.044
161
NVS015 Nevus Comedonicus 39 0.044
162
CRV045 Cervical Intraepithelial Neoplasia 39 0.044
163
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.044
164
NCR002 Necrobiosis Lipoidica 38 0.044
165
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.044
166
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.044
167
FCL001 Facial Dermatosis 29 0.044
168
FXF002 Fox-Fordyce Disease 27 0.044
169
HDG004 Hodgkin's Granuloma 26 0.044
170
HDG006 Hodgkin's Paragranuloma 24 0.044
171
P PRS040 Prostate Cancer 97 0.031
172
P BRS047 Breast Cancer 96 0.031
173
ESP021 Esophageal Cancer 90 0.031
174
P ALZ034 Alzheimer Disease 88 0.031
175
P PNC035 Pancreatic Cancer 84 0.031
176
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.031
177
c LKM071 Leukemia, Chronic Lymphocytic 79 0.031
178
IMM167 Immune Deficiency Disease 78 0.031
179
P MDL005 Medulloblastoma 77 0.031
180
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.031
181
P HRT032 Heart Disease 75 0.031
182
P SCH015 Schizophrenia 75 0.031
183
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.031
184
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.031
185
ANX010 Anxiety 72 0.031
186
P MLT020 Multiple Sclerosis 72 0.031
187
c HYP836 Hypercholesterolemia, Familial, 1 72 0.031
188
BSL036 Basal Cell Nevus Syndrome 72 0.031
189
P PHC003 Pheochromocytoma 71 0.031
190
PRP027 Peripheral Vascular Disease 71 0.031
191
P KDN018 Kidney Disease 70 0.031
192
P ART022 Arthritis 70 0.031
193
PLY001 Polycythemia Vera 69 0.031
194
c MGR028 Migraine with or Without Aura 1 69 0.031
195
RCK004 Rickets 69 0.031
196
c EXD008 Exudative Vitreoretinopathy 1 69 0.031
197
P OCL013 Oculodentodigital Dysplasia 69 0.031
198
P LVR013 Liver Disease 68 0.031
199
EWN003 Ewing Sarcoma 68 0.031
200
BRN024 Bronchitis 68 0.031
201
P INF038 Influenza 68 0.031
202
KRT019 Keratitis, Hereditary 67 0.031
203
PNC129 Pancreatic Adenocarcinoma 67 0.031
204
MYL005 Myelofibrosis 67 0.031
205
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.031
206
CHL065 Cholangiocarcinoma 67 0.031
207
ALL003 Allergic Rhinitis 67 0.031
208
P NSP012 Nasopharyngeal Carcinoma 67 0.031
209
SVR097 Severe Cutaneous Adverse Reaction 67 0.031
210
P DRM053 Dermatitis, Atopic 66 0.031
211
FBR011 Fibrodysplasia Ossificans Progressiva 66 0.031
212
ALC007 Alcohol Dependence 66 0.031
213
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.031
214
P MCR115 Microvascular Complications of Diabetes 5 66 0.031
215
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.031
216
c MCR129 Microvascular Complications of Diabetes 1 66 0.031
217
P NRV007 Nervous System Disease 66 0.031
218
ATH013 Atherosclerosis Susceptibility 66 0.031
219
LNG039 Lung Squamous Cell Carcinoma 65 0.031
220
P BLD062 Bile Duct Cancer 65 0.031
221
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.031
222
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.031
223
c WLM013 Wilms Tumor 1 65 0.031
224
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.031
225
INC002 Inclusion Body Myositis 64 0.031
226
CLF027 Cleft Palate, Isolated 64 0.031
227
DSM004 Desmoid Tumor 64 0.031
228
TTN003 Tetanus 64 0.031
229
CLN015 Colon Adenocarcinoma 63 0.031
230
RHB001 Rhabdoid Cancer 63 0.031
231
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.031
232
DPR016 Depression 63 0.031
233
LVR012 Liver Cirrhosis 63 0.031
234
P MST009 Mastocytosis 63 0.031
235
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.031
236
c SCL052 Scleroderma, Familial Progressive 62 0.031
237
P RHB003 Rhabdomyosarcoma 62 0.031
238
c WLM018 Wilms Tumor 5 62 0.031
239
BLL006 Bullous Pemphigoid 62 0.031
240
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.031
241
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.031
242
NTR005 Nutritional Deficiency Disease 61 0.031
243
OSS012 Osseous Heteroplasia, Progressive 61 0.031
244
ATY005 Atypical Teratoid Rhabdoid Tumor 61 0.031
245
P LPS004 Lupus Erythematosus 61 0.031
246
P MCR256 Microphthalmia, Syndromic 9 61 0.031
247
LNG099 Lung Disease 61 0.031
248
LYM012 Lymphoplasmacytic Lymphoma 61 0.031
249
DRR014 Darier-White Disease 61 0.031
250
P LYM033 Lymphoproliferative Syndrome 60 0.031
251
c PCH015 Pachyonychia Congenita 1 60 0.031
252
ACQ007 Acquired Immunodeficiency Syndrome 60 0.031
253
PNM010 Pneumothorax, Primary Spontaneous 60 0.031
254
ORL011 Oral Cancer 60 0.031
255
P PTN014 Patent Ductus Arteriosus 1 60 0.031
256
P ECT006 Ectodermal Dysplasia 59 0.031
257
THY029 Thyroid Carcinoma 59 0.031
258
WHM001 Whim Syndrome 59 0.031
259
PBL005 Piebald Trait 59 0.031
260
IGR001 Ige Responsiveness, Atopic 59 0.031
261
PRL032 Perlman Syndrome 58 0.031
262
CRV038 Cervical Squamous Cell Carcinoma 58 0.031
263
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.031
264
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58 0.031
265
P ALC033 Alcohol Use Disorder 58 0.031
266
THY122 Thyroid Gland Cancer 58 0.031
267
P BCL017 B-Cell Lymphoma 58 0.031
268
ADR005 Adrenal Carcinoma 58 0.031
269
c CHL119 Cholangitis, Primary Sclerosing 57 0.031
270
ERY003 Erythema Multiforme 57 0.031
271
P INF032 Infertility 57 0.031
272
P RHN004 Rhinitis 57 0.031
273
P HDC001 Headache 57 0.031
274
P UVT001 Uveitis 57 0.031
275
ENC044 Enchondromatosis, Multiple, Ollier Type 57 0.031
276
P PRP019 Peripheral Nervous System Disease 57 0.031
277
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.031
278
MNT002 Mental Depression 57 0.031
279
P DRR001 Diarrhea 57 0.031
280
c ADL017 Adult T-Cell Leukemia 57 0.031
281
P SJG008 Sjogren Syndrome 56 0.031
282
P PNL012 Penile Cancer 56 0.031
283
P NRP001 Neuropathy 56 0.031
284
THR024 Thrombosis 56 0.031
285
SPN041 Spinal Cord Disease 56 0.031
286
TRN018 Transitional Cell Carcinoma 56 0.031
287
PLS011 Plasmacytoma 56 0.031
288
ALP097 Alopecia Universalis Congenita 56 0.031
289
HYP266 Hypoxia 56 0.031
290
SFT003 Soft Tissue Sarcoma 56 0.031
291
ISL001 Islet Cell Tumor 56 0.031
292
P MLN007 Male Infertility 56 0.031
293
SKN022 Skin Squamous Cell Carcinoma 56 0.031
294
PNM008 Pneumothorax 56 0.031
295
EPD002 Epidermolytic Hyperkeratosis 56 0.031
296
DFF005 Diffuse Large B-Cell Lymphoma 56 0.031
297
P PLM034 Pulmonary Emphysema 56 0.031
298
ICH001 Ichthyosis Vulgaris 55 0.031
299
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.031
300
HYP005 Hypokalemia 55 0.031
301
MCS002 Mucositis 55 0.031
302
MCL006 Macular Retinal Edema 55 0.031
303
P PLY018 Polycythemia 55 0.031
304
HYP691 Hypomelanosis of Ito 55 0.031
305
CPL003 Capillary Leak Syndrome 55 0.031
306
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.031
307
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.031
308
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.031
309
PRN019 Perinatal Necrotizing Enterocolitis 54 0.031
310
CRT017 Cartilage Disease 54 0.031
311
c CNT035 Central Nervous System Disease 54 0.031
312
c PST005 Posterior Uveitis 54 0.031
313
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.031
314
CHR100 Chronic Ulcer of Skin 53 0.031
315
CLR030 Clear Cell Renal Cell Carcinoma 53 0.031
316
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.031
317
INT075 Intracranial Hypertension 53 0.031
318
MMM001 Mammary Paget's Disease 53 0.031
319
P HYP730 Hypogonadotropic Hypogonadism 53 0.031
320
KRT006 Keratoconjunctivitis 53 0.031
321
P RTN018 Retinal Disease 52 0.031
322
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.031
323
ACR041 Acromelic Frontonasal Dysostosis 52 0.031
324
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.031
325
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.031
326
DRM011 Dermatophytosis 52 0.031
327
P INS002 in Situ Carcinoma 52 0.031
328
c EXS019 Exostoses, Multiple, Type I 52 0.031
329
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.031
330
c PRM012 Primary Polycythemia 52 0.031
331
c PSR017 Psoriasis 2 52 0.031
332
SPP010 Suppressor of Tumorigenicity 3 51 0.031
333
PNG002 Pain Agnosia 51 0.031
334
AZS001 Azoospermia 50 0.031
335
HYP081 Hypolipoproteinemia 50 0.031
336
ENT011 Enterocolitis 50 0.031
337
c GCH016 Gaucher Disease, Type Ii 50 0.031
338
P CHL066 Cholangitis 50 0.031
339
c CHR418 Chronic Leukemia 50 0.031
340
c INF145 Infantile Liver Failure Syndrome 1 50 0.031
341
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.031
342
P PNB001 Pineoblastoma 50 0.031
343
MCR004 Macroglobulinemia 50 0.031
344
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.031
345
P CTN015 Cutaneous T Cell Lymphoma 49 0.031
346
MNL001 Monilethrix 49 0.031
347
CHL018 Childhood Medulloblastoma 49 0.031
348
c PSR023 Psoriasis 1 49 0.031
349
RTC005 Reticulosarcoma 49 0.031
350
CHL056 Cheilitis 48 0.031
351
P KRT005 Keratoacanthoma 48 0.031
352
INT054 Intraocular Lymphoma 48 0.031
353
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.031
354
PLM029 Palmoplantar Keratosis 47 0.031
355
GNG008 Ganglioneuroblastoma 47 0.031
356
DRY001 Dry Eye Syndrome 47 0.031
357
c MCR120 Microvascular Complications of Diabetes 7 47 0.031
358
P SCL009 Sclerosing Cholangitis 47 0.031
359
P TCL004 T-Cell Leukemia 47 0.031
360
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.031
361
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.031
362
EXS001 Exostosis 46 0.031
363
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.031
364
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.031
365
ADR040 Adrenal Gland Pheochromocytoma 46 0.031
366
P HRD001 Hereditary Multiple Exostoses 46 0.031
367
TRT001 Teratocarcinoma 46 0.031
368
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.031
369
P EPN001 Ependymoblastoma 45 0.031
370
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.031
371
PNC056 Pineocytoma 45 0.031
372
P OST028 Osteochondroma 45 0.031
373
LYM051 Lymphomatoid Granulomatosis 45 0.031
374
PGM003 Pigmentation Disease 44 0.031
375
BZX001 Bazex Syndrome 44 0.031
376
MRG013 Mirage Syndrome 44 0.031
377
CYT002 Cytokine Deficiency 44 0.031
378
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.031
379
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.031
380
c RTN047 Retinitis Pigmentosa 18 44 0.031
381
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.031
382
c HYP272 Hypercholesterolemia, Familial, 3 43 0.031
383
P BLD036 Bile Duct Disease 43 0.031
384
TRP009 Triple X Syndrome 42 0.031
385
XRP001 Xerophthalmia 42 0.031
386
P ECT005 Ectropion 41 0.031
387
GST020 Gastric Antral Vascular Ectasia 41 0.031
388
c NLD016 Nail Disorder, Nonsyndromic Congenital, 10 41 0.031
389
CTN004 Cutaneous Fibrous Histiocytoma 41 0.031
390
c MCR112 Microvascular Complications of Diabetes 2 41 0.031
391
P RRT020 Rare Tumor 41 0.031
392
PYG006 Pyogenic Granuloma 40 0.031
393
PNS010 Penis Squamous Cell Carcinoma 40 0.031
394
MYS001 Myositis Ossificans 40 0.031
395
PNL014 Pineal Gland Cancer 40 0.031
396
ERM002 Ear Malformation 39 0.031
397
c MLG157 Malignant Pheochromocytoma 39 0.031
398
c HRD104 Hereditary Multiple Osteochondromas 39 0.031
399
c MLG074 Malignant Mesenchymoma 39 0.031
400
c PSR028 Psoriasis 7 39 0.031
401
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 39 0.031
402
c CHR682 Chronic Bilirubin Encephalopathy 38 0.031
403
P FML361 Familial Woolly Hair Syndrome 38 0.031
404
c PSR032 Psoriasis 11 38 0.031
405
c PSR018 Psoriasis 13 38 0.031
406
PRN039 Paraneoplastic Syndromes 38 0.031
407
PTY002 Pityriasis Versicolor 37 0.031
408
P SYR003 Syringoma 37 0.031
409
KLD003 Keloid Formation 37 0.031
410
c WLM011 Wilms Tumor 6 37 0.031
411
PMP010 Pompholyx 37 0.031
412
HRY002 Hairy Tongue 36 0.031
413
OLG022 Oligoasthenoteratozoospermia 36 0.031
414
TNM001 Tinea Imbricata 36 0.031
415
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.031
416
CRB026 Cerebellar Astrocytoma 35 0.031
417
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.031
418
LNR004 Linear Porokeratosis 35 0.031
419
INF057 Inflammatory Linear Verrucous Epidermal Nevus 34 0.031
420
47X003 47, Xxy 34 0.031
421
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 33 0.031
422
BCK005 Becker Nevus Syndrome 33 0.031
423
c NNN025 Noonan Syndrome 10 33 0.031
424
c PRS136 Prostate Cancer, Hereditary, 6 33 0.031
425
NVS007 Nevus of Ota 33 0.031
426
c PRS130 Prostate Cancer, Hereditary, 8 32 0.031
427
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.031
428
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.031
429
ALP048 Alopecia Totalis 31 0.031
430
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.031
431
ATR054 Atrophoderma Vermiculata 29 0.031
432
MLG163 Malignant Tumor of Penis 29 0.031
433
PST092 Posttransplant Acute Limbic Encephalitis 29 0.031
434
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.031
435
ERY066 Erythema Multiforme Major 28 0.031
436
P OVR096 Overlap Myositis 27 0.031
437
HYP160 Hyperkeratosis Lenticularis Perstans 27 0.031
438
CYT018 Cytochrome P450 2d6 Variant 27 0.031
439
HYP855 Hyperpigmentation of the Skin 27 0.031
440
CHL079 Children's Interstitial Lung Disease 27 0.031
441
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 26 0.031
442
ANG061 Angular Cheilitis 26 0.031
443
NDL011 Nodular Ganglioneuroblastoma 25 0.031
444
MRP002 Morpheaform Basal Cell Carcinoma 24 0.031
445
ERS002 Erosive Pustular Dermatosis of the Scalp 23 0.031
446
KYR001 Kyrle Disease 23 0.031
447
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.031
448
IST006 Isotretinoin Syndrome 22 0.031
449
CLL040 Callosities, Hereditary Painful 18 0.031
450
HDR007 Hidrotic Ectodermal Dysplasia 2 16 0.031
451
TRC061 Trichostasis Spinulosa 14 0.031
452
CHL009 Childhood Cerebral Astrocytoma 14 0.031
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