Search results for Tretinoin

539 hits were found for Tretinoin

# Family MCID Name MIFTS Score
1
P ACN011 Acne 55 19.744
2
c DWL002 Dowling-Degos Disease 1 58 9.123
3
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 34 6.858
4
ACT119 Acute Promyelocytic Leukemia 62 6.598
5
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 34 6.243
6
P LKM002 Leukemia 66 5.724
7
LNT004 Lentigines 45 5.061
8
KRT009 Keratosis 52 4.725
9
c FNC043 Fanconi Anemia, Complementation Group E 62 4.163
10
SKN016 Skin Disease 62 3.974
11
c BSL007 Basal Cell Carcinoma 68 3.923
12
RSC001 Rosacea 55 3.753
13
c LKM061 Leukemia, Acute Myeloid 83 3.737
14
P MYL006 Myeloid Leukemia 60 3.598
15
NRR001 Neuroretinitis 42 3.564
16
RTN023 Retinitis 45 3.564
17
P ACT008 Actinic Keratosis 54 3.536
18
MYL009 Myelodysplastic Syndrome 67 3.464
19
P MLN008 Melanoma 75 3.257
20
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 3.040
21
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 3.040
22
AGN016 Aging 54 2.801
23
P SKN015 Skin Carcinoma 71 2.781
24
P ALP008 Alopecia 53 2.711
25
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 2.710
26
48X005 48,xyyy 39 2.624
27
ANT039 Antisynthetase Syndrome 55 2.617
28
DRM006 Dermatitis 62 2.581
29
IRR003 Irritant Dermatitis 47 2.519
30
CNT047 Contact Dermatitis 57 2.509
31
P LCH002 Lichen Planus 55 2.470
32
PST011 Pustulosis of Palm and Sole 52 2.440
33
P PSR002 Psoriasis 63 2.440
34
ADL002 Adult Syndrome 69 2.404
35
SQM006 Squamous Cell Carcinoma 59 2.383
36
ACT113 Acute Myeloblastic Leukemia with Maturation 46 2.373
37
c CHR064 Chronic Monocytic Leukemia 36 2.360
38
DYS002 Dysplastic Nevus Syndrome 54 2.264
39
MLN073 Melanosis, Neurocutaneous 45 2.261
40
ACN002 Acanthosis Nigricans 56 2.245
41
RNL114 Renal Cell Carcinoma, Nonpapillary 79 2.125
42
SKN005 Skin Atrophy 41 2.106
43
P TRN020 Turner Syndrome 67 2.020
44
P LNG032 Lung Cancer 98 1.918
45
KRT002 Keratomalacia 54 1.866
46
AND014 Androgenic Alopecia 46 1.832
47
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.813
48
P ICH004 Ichthyosis 56 1.767
49
LKP003 Leukoplakia 39 1.754
50
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.719
51
P LTR001 Lateral Sclerosis 58 1.719
52
P LYM118 Lymphoma 69 1.706
53
LYM019 Lymphosarcoma 46 1.706
54
P BLD134 Bladder Cancer 79 1.681
55
TLN003 Telangiectasis 51 1.676
56
KRT001 Keratoconjunctivitis Sicca 49 1.671
57
ORL013 Oral Lichen Planus 45 1.646
58
HYP457 Hypertrophic Scars 42 1.628
59
P FNG006 Feingold Syndrome 1 61 1.616
60
PPL022 Papilloma 53 1.614
61
P ANR048 Aniridia 1 66 1.591
62
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 1.591
63
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 1.591
64
INT002 Intermittent Claudication 61 1.591
65
P MTR014 Motor Neuron Disease 65 1.591
66
KLD004 Keloid Disorder 39 1.583
67
ACT250 Acute Megakaryocytic Leukemia 63 1.575
68
LCH016 Lichen Sclerosus Et Atrophicus 41 1.571
69
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.571
70
P ADN016 Adenocarcinoma 63 1.570
71
SVR001 Severe Acute Respiratory Syndrome 68 1.523
72
ORL012 Oral Leukoplakia 35 1.523
73
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.522
74
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 1.522
75
P ALP061 Alopecia, Androgenetic, 1 49 1.454
76
ERY051 Erythroleukemia, Familial 37 1.394
77
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.394
78
MYC006 Mycosis Fungoides 65 1.394
79
DWN001 Down Syndrome 70 1.394
80
c BSL024 Basal Cell Carcinoma 1 54 1.394
81
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.394
82
P MLN066 Melanoma, Cutaneous Malignant 1 66 1.394
83
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 63 1.394
84
MLN065 Melanocytic Nevus Syndrome, Congenital 61 1.394
85
c LKM070 Leukemia, Acute Monocytic 56 1.394
86
FNG017 Fungal Infectious Disease 54 1.394
87
PHT004 Photoallergic Dermatitis 27 1.394
88
SKN013 Skin Benign Neoplasm 49 1.394
89
SKN019 Skin Melanoma 70 1.394
90
SZR001 Sezary's Disease 60 1.394
91
P CNJ013 Conjunctivitis 66 1.335
92
P SRC025 Sarcoidosis 1 70 1.335
93
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 1.333
94
MYL031 Myeloproliferative Neoplasm 66 1.333
95
BNM001 Bone Marrow Cancer 45 1.333
96
PLS009 Plasma Cell Neoplasm 64 1.311
97
P HYP058 Hypervitaminosis a 47 1.304
98
ALL010 Allergic Contact Dermatitis 56 1.304
99
MLL001 Molluscum Contagiosum 48 1.304
100
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.269
101
P LNG064 Lung Cancer Susceptibility 3 70 1.254
102
KPS004 Kaposi Sarcoma 76 1.230
103
LYM133 Lymphoma, Hodgkin, Classic 74 1.206
104
c SML038 Small Cell Cancer of the Lung 69 1.206
105
LNG031 Lung Benign Neoplasm 51 1.206
106
HDG004 Hodgkin's Granuloma 22 1.206
107
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 1.206
108
HDG006 Hodgkin's Paragranuloma 21 1.206
109
P CHR285 Chronic Myelomonocytic Leukemia 59 1.205
110
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 1.205
111
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 1.205
112
RFR007 Refractory Anemia with Excess Blasts in Transformation 26 1.205
113
WHM001 Whim Syndrome 60 1.189
114
P OST002 Osteoporosis 77 1.187
115
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.187
116
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.187
117
MRP002 Morpheaform Basal Cell Carcinoma 24 1.187
118
IMM167 Immune Deficiency Disease 77 1.148
119
P ALP009 Alopecia Areata 59 1.148
120
P NTR004 Neutropenia 62 1.145
121
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.139
122
P PRK001 Porokeratosis 54 1.139
123
THR004 Thrombocytosis 52 1.115
124
NVS015 Nevus Comedonicus 38 1.111
125
PYG006 Pyogenic Granuloma 36 1.111
126
P GRF003 Graft-Versus-Host Disease 71 1.095
127
P MYS005 Myositis 56 1.095
128
NCR002 Necrobiosis Lipoidica 39 1.081
129
ACT011 Acute Contagious Conjunctivitis 42 1.079
130
CLF027 Cleft Palate, Isolated 64 1.063
131
MYL069 Myeloma, Multiple 77 1.055
132
ATY042 Atypical Chronic Myeloid Leukemia 50 1.055
133
HMT002 Hematologic Cancer 61 1.055
134
P PNC035 Pancreatic Cancer 86 1.040
135
P NRB001 Neuroblastoma 66 1.040
136
AMD002 Amed Syndrome, Digenic 37 1.017
137
ANG049 Angioedema Induced by Ace Inhibitors 39 1.010
138
P AMY004 Amyloidosis 69 1.008
139
PST092 Posttransplant Acute Limbic Encephalitis 29 1.008
140
c ATS013 Autosomal Recessive Congenital Ichthyosis 65 1.006
141
NVS017 Nevus, Epidermal 66 1.006
142
MCL047 Macular Amyloidosis 19 0.988
143
CRV035 Cervical Cancer 72 0.987
144
P LKM071 Leukemia, Chronic Lymphocytic 74 0.987
145
P KDN017 Kidney Cancer 60 0.987
146
IST006 Isotretinoin Syndrome 20 0.981
147
P PRM001 Primary Cutaneous Amyloidosis 47 0.968
148
FXF002 Fox-Fordyce Disease 26 0.953
149
MCS002 Mucositis 55 0.946
150
CHR100 Chronic Ulcer of Skin 57 0.946
151
KRT006 Keratoconjunctivitis 53 0.946
152
ORL011 Oral Cancer 60 0.946
153
KLD003 Keloid Formation 34 0.922
154
PMP014 Pemphigoid 49 0.897
155
ERY003 Erythema Multiforme 56 0.897
156
PRP027 Peripheral Vascular Disease 71 0.897
157
P DRR001 Diarrhea 55 0.897
158
CHL056 Cheilitis 46 0.897
159
c RTN047 Retinitis Pigmentosa 18 45 0.897
160
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.870
161
XRP001 Xerophthalmia 42 0.870
162
SVR097 Severe Cutaneous Adverse Reaction 68 0.870
163
ANG061 Angular Cheilitis 27 0.870
164
CTN004 Cutaneous Fibrous Histiocytoma 39 0.870
165
ERY066 Erythema Multiforme Major 29 0.870
166
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.870
167
P PRS040 Prostate Cancer 95 0.858
168
P BRS047 Breast Cancer 97 0.858
169
MYL005 Myelofibrosis 70 0.858
170
c LKM063 Leukemia, Chronic Myeloid 71 0.858
171
P LKM062 Leukemia, Acute Lymphoblastic 69 0.858
172
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.858
173
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.858
174
ADN011 Adenoid Cystic Carcinoma 68 0.858
175
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 0.858
176
ADN002 Adenoiditis 36 0.858
177
JVN004 Juvenile Myelomonocytic Leukemia 67 0.858
178
LYM040 Lymphoblastic Lymphoma 53 0.858
179
P CRV039 Cervicitis 52 0.858
180
ART109 Arterial Thoracic Outlet Syndrome 24 0.858
181
RFR010 Refractory Anemia 49 0.858
182
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.839
183
DSM004 Desmoid Tumor 65 0.839
184
KYR001 Kyrle Disease 22 0.839
185
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.839
186
LNR004 Linear Porokeratosis 33 0.839
187
ALP097 Alopecia Universalis Congenita 57 0.805
188
PLM029 Palmoplantar Keratosis 48 0.805
189
ALP048 Alopecia Totalis 31 0.805
190
PTY002 Pityriasis Versicolor 37 0.805
191
NVS007 Nevus of Ota 28 0.805
192
HYP855 Hyperpigmentation of the Skin 26 0.805
193
c NNN025 Noonan Syndrome 10 31 0.764
194
SRC014 Sarcoma 64 0.764
195
ICH001 Ichthyosis Vulgaris 53 0.764
196
ACQ007 Acquired Immunodeficiency Syndrome 58 0.764
197
P ECT006 Ectodermal Dysplasia 62 0.764
198
SPN035 Spindle Cell Sarcoma 51 0.764
199
INF057 Inflammatory Linear Verrucous Epidermal Nevus 33 0.764
200
INT075 Intracranial Hypertension 52 0.764
201
HDR007 Hidrotic Ectodermal Dysplasia 2 21 0.764
202
FCL001 Facial Dermatosis 35 0.743
203
P DRM053 Dermatitis, Atopic 65 0.723
204
BSL036 Basal Cell Nevus Syndrome 73 0.711
205
TNM001 Tinea Imbricata 42 0.711
206
INT303 Intracranial Hypertension, Idiopathic 56 0.711
207
HYP160 Hyperkeratosis Lenticularis Perstans 27 0.711
208
EPD002 Epidermolytic Hyperkeratosis 55 0.711
209
c SCL052 Scleroderma, Familial Progressive 60 0.711
210
P SYR003 Syringoma 36 0.711
211
MMM001 Mammary Paget's Disease 53 0.711
212
BZX001 Bazex Syndrome 45 0.711
213
TRC061 Trichostasis Spinulosa 13 0.711
214
P INS002 in Situ Carcinoma 53 0.711
215
PRN039 Paraneoplastic Syndromes 37 0.711
216
DRM011 Dermatophytosis 52 0.711
217
c CHR417 Chronic Graft Versus Host Disease 55 0.711
218
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 36 0.711
219
P RRT020 Rare Tumor 39 0.711
220
ATR054 Atrophoderma Vermiculata 40 0.583
221
PRT251 Proteinuria, Chronic Benign 58 0.583
222
P FML361 Familial Woolly Hair Syndrome 49 0.583
223
CLL040 Callosities, Hereditary Painful 18 0.583
224
DRR014 Darier-White Disease 58 0.583
225
MNL001 Monilethrix 48 0.583
226
ERM002 Ear Malformation 35 0.583
227
IGR001 Ige Responsiveness, Atopic 59 0.583
228
P ECT005 Ectropion 41 0.583
229
P PRP019 Peripheral Nervous System Disease 57 0.583
230
HRY002 Hairy Tongue 28 0.583
231
P KRT005 Keratoacanthoma 47 0.583
232
P RHB003 Rhabdomyosarcoma 66 0.583
233
P NRP001 Neuropathy 59 0.583
234
ERS002 Erosive Pustular Dermatosis of the Scalp 21 0.583
235
PGM003 Pigmentation Disease 45 0.565
236
P CTN015 Cutaneous T Cell Lymphoma 48 0.565
237
PNC129 Pancreatic Adenocarcinoma 65 0.565
238
P LVR013 Liver Disease 68 0.565
239
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.565
240
P CNR004 Cone-Rod Dystrophy 2 75 0.512
241
c PCH015 Pachyonychia Congenita 1 60 0.512
242
NTR018 Neutrophilia, Hereditary 49 0.512
243
P ALC033 Alcohol Use Disorder 67 0.512
244
P RTN018 Retinal Disease 53 0.512
245
SQM002 Squamous Cell Papilloma 45 0.512
246
ALL029 Allergic Disease 61 0.512
247
P ALZ034 Alzheimer Disease 87 0.384
248
P SCH015 Schizophrenia 74 0.384
249
ESP021 Esophageal Cancer 84 0.384
250
CHN019 Chand Syndrome 31 0.384
251
P SPP010 Suppressor of Tumorigenicity 3 51 0.384
252
PLY001 Polycythemia Vera 69 0.384
253
PRL032 Perlman Syndrome 57 0.384
254
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.384
255
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.384
256
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.384
257
c MCR115 Microvascular Complications of Diabetes 5 65 0.384
258
CRN241 Corneal Dystrophy, Congenital Stromal 49 0.384
259
c PSR032 Psoriasis 11 47 0.384
260
BCK005 Becker Nevus Syndrome 33 0.384
261
c WLM011 Wilms Tumor 6 25 0.384
262
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.384
263
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.384
264
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.384
265
P ADL017 Adult T-Cell Leukemia 54 0.384
266
MNT001 Mantle Cell Lymphoma 65 0.384
267
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.384
268
PRP036 Peripheral T-Cell Lymphoma 52 0.384
269
P HYP730 Hypogonadotropic Hypogonadism 54 0.384
270
RCK004 Rickets 65 0.384
271
c PRM012 Primary Polycythemia 58 0.384
272
MLG157 Malignant Pheochromocytoma 37 0.384
273
CVD001 Covid-19 58 0.384
274
P MDL005 Medulloblastoma 75 0.384
275
c MGR028 Migraine with or Without Aura 1 64 0.384
276
ENC044 Enchondromatosis, Multiple, Ollier Type 56 0.384
277
ALC007 Alcohol Dependence 65 0.384
278
BRK010 Burkitt Lymphoma 66 0.384
279
P MLT020 Multiple Sclerosis 79 0.384
280
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.384
281
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.384
282
HYP781 Hypoascorbemia 52 0.384
283
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.384
284
c PSR023 Psoriasis 1 52 0.384
285
ADR040 Adrenal Gland Pheochromocytoma 45 0.384
286
P LYM033 Lymphoproliferative Syndrome 59 0.384
287
LYM012 Lymphoplasmacytic Lymphoma 50 0.384
288
P FLL037 Follicular Lymphoma 73 0.384
289
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.384
290
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.384
291
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.384
292
c HYP272 Hypercholesterolemia, Familial, 3 46 0.384
293
HMN044 Human Immunodeficiency Virus Type 1 76 0.384
294
c PRS130 Prostate Cancer, Hereditary, 8 32 0.384
295
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.384
296
c PRS136 Prostate Cancer, Hereditary, 6 33 0.384
297
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.384
298
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.384
299
c HYP836 Hypercholesterolemia, Familial, 1 73 0.384
300
INC002 Inclusion Body Myositis 57 0.384
301
KRT013 Keratolytic Winter Erythema 45 0.384
302
c EXS019 Exostoses, Multiple, Type I 54 0.384
303
c EXD008 Exudative Vitreoretinopathy 1 71 0.384
304
P CMP005 Campomelic Dysplasia 65 0.384
305
OSS012 Osseous Heteroplasia, Progressive 61 0.384
306
P PHC003 Pheochromocytoma 70 0.384
307
PBL005 Piebald Trait 59 0.384
308
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.384
309
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.384
310
FLL041 Follicular Lymphoma 1 44 0.384
311
c CHL119 Cholangitis, Primary Sclerosing 57 0.384
312
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.384
313
c PSR018 Psoriasis 13 40 0.384
314
c PSR028 Psoriasis 7 43 0.384
315
c WLM018 Wilms Tumor 5 54 0.384
316
P SJG008 Sjogren Syndrome 61 0.384
317
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 53 0.384
318
EWN003 Ewing Sarcoma 70 0.384
319
c INF145 Infantile Liver Failure Syndrome 1 44 0.384
320
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 72 0.384
321
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 57 0.384
322
c WLM013 Wilms Tumor 1 65 0.384
323
P PRS038 Personality Disorder 65 0.384
324
EXS001 Exostosis 49 0.384
325
ANG046 Angioimmunoblastic T-Cell Lymphoma 51 0.384
326
DRY001 Dry Eye Syndrome 49 0.384
327
WLD007 Waldenstroem's Macroglobulinemia 65 0.384
328
PLS025 Plasmablastic Lymphoma 56 0.384
329
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.384
330
DFC004 Deficiency Anemia 74 0.384
331
c HPT003 Hepatitis a 63 0.384
332
c ACT073 Acute Leukemia 59 0.384
333
MLG169 Malignant Astrocytoma 57 0.384
334
c ACT027 Acute Pancreatitis 60 0.384
335
GRM005 Germ Cell Cancer 46 0.384
336
MYS001 Myositis Ossificans 44 0.384
337
P INF032 Infertility 60 0.384
338
P PNC044 Pancreatitis 61 0.384
339
NTR005 Nutritional Deficiency Disease 60 0.384
340
NDL011 Nodular Ganglioneuroblastoma 25 0.384
341
P HPT021 Hepatitis 68 0.384
342
P PNB001 Pineoblastoma 49 0.384
343
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.384
344
TRN018 Transitional Cell Carcinoma 56 0.384
345
MNT002 Mental Depression 56 0.384
346
BRN028 Brain Cancer 73 0.384
347
HNT002 Hantavirus Pulmonary Syndrome 55 0.384
348
PRS047 Prostatitis 58 0.384
349
ISL001 Islet Cell Tumor 55 0.384
350
AZS001 Azoospermia 45 0.384
351
P SCL009 Sclerosing Cholangitis 46 0.384
352
HMN048 Human Papillomavirus Infectious Disease 46 0.384
353
P MLN007 Male Infertility 56 0.384
354
PNL012 Penile Cancer 57 0.384
355
GLS001 Gliosarcoma 63 0.384
356
SKN022 Skin Squamous Cell Carcinoma 54 0.384
357
P OLG002 Oligodendroglioma 66 0.384
358
RHB001 Rhabdoid Cancer 68 0.384
359
PLS011 Plasmacytoma 56 0.384
360
LNG039 Lung Squamous Cell Carcinoma 57 0.384
361
P RHN004 Rhinitis 57 0.384
362
CRV038 Cervical Squamous Cell Carcinoma 56 0.384
363
P HRD001 Hereditary Multiple Exostoses 48 0.384
364
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.384
365
ANP005 Anaplastic Astrocytoma 59 0.384
366
ART002 Arts Syndrome 66 0.384
367
c PSR017 Psoriasis 2 53 0.384
368
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.384
369
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.384
370
SCH036 Scheie Syndrome 73 0.384
371
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.384
372
HYP691 Hypomelanosis of Ito 53 0.384
373
DPR016 Depression 65 0.384
374
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 35 0.384
375
OLG022 Oligoasthenoteratozoospermia 35 0.384
376
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 43 0.384
377
CYT002 Cytokine Deficiency 43 0.384
378
LYM048 Lymphoma, Large-Cell, Immunoblastic 27 0.384
379
RTC005 Reticulosarcoma 47 0.384
380
P PLY018 Polycythemia 56 0.384
381
P MXD050 Mixed Phenotype Acute Leukemia 45 0.384
382
HRD104 Hereditary Multiple Osteochondromas 43 0.384
383
LNG099 Lung Disease 62 0.384
384
CRH001 Crohn's Disease 80 0.384
385
GNG008 Ganglioneuroblastoma 46 0.384
386
PNS010 Penis Squamous Cell Carcinoma 45 0.384
387
CLR030 Clear Cell Renal Cell Carcinoma 54 0.384
388
P EPN001 Ependymoblastoma 44 0.384
389
PNL014 Pineal Gland Cancer 40 0.384
390
P HDC001 Headache 56 0.384
391
P PLM034 Pulmonary Emphysema 58 0.384
392
P RCR004 Recurrent Respiratory Papillomatosis 48 0.384
393
AND005 Androgen Insensitivity Syndrome, Mild 21 0.384
394
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.384
395
PMP010 Pompholyx 33 0.384
396
P BCL017 B-Cell Lymphoma 57 0.384
397
INT054 Intraocular Lymphoma 48 0.384
398
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.384
399
P CHL066 Cholangitis 51 0.384
400
c LKM005 Leukemia, T-Cell, Chronic 33 0.384
401
LYM051 Lymphomatoid Granulomatosis 44 0.384
402
P OST028 Osteochondroma 44 0.384
403
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.384
404
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.384
405
PNC056 Pineocytoma 44 0.384
406
MCR004 Macroglobulinemia 48 0.384
407
c PRM038 Primary Agammaglobulinemia 47 0.384
408
TCL024 T-Cell Non-Hodgkin Lymphoma 39 0.384
409
P OVR096 Overlap Myositis 27 0.384
411
CHR682 Chronic Bilirubin Encephalopathy 37 0.384
412
CLS016 Clostridium Difficile Colitis 49 0.314
413
OCH001 Ochronosis 40 0.314
414
P PLY019 Polyneuropathy 53 0.256
415
c HPT001 Hepatitis C 61 0.256
416
PMS001 Poems Syndrome 59 0.256
417
FLL008 Folliculitis 45 0.256
418
CHR072 Chordoma 57 0.222
419
DSS009 Disseminated Intravascular Coagulation 56 0.222
420
P PLY011 Polycystic Ovary Syndrome 57 0.222
421
BWN006 Bowen's Disease 32 0.222
422
FTL028 Fetal Retinoid Syndrome 14 0.222
423
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.222
424
PRM329 Premature Aging 36 0.222
425
P OVR082 Overgrowth Syndrome 42 0.222
426
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.181
427
P CRD119 Cardiac Arrest 68 0.181
428
FDB001 Foodborne Botulism 55 0.181
429
IFP003 Ifap Syndrome 2 42 0.181
430
ELS002 Elastosis Perforans Serpiginosa 33 0.181
431
EPD070 Epidermoid Cysts 35 0.181
432
NRL016 Neural Tube Defects 81 0.181
433
CRD223 Cardiac Arrhythmia 63 0.181
434
URM002 Uremia 47 0.181
435
P MCR010 Microcephaly 59 0.181
436
c ACT071 Acute Kidney Failure 60 0.181
437
GRN007 Granuloma Annulare 43 0.181
438
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.181
439
P KDN018 Kidney Disease 72 0.181
440
BLL006 Bullous Pemphigoid 61 0.181
441
BLP005 Blepharitis 50 0.181
442
LCH008 Lichen Planus Pigmentosus 23 0.181
443
P PMP001 Pemphigus 55 0.181
444
CYS001 Cystic Fibrosis 77 0.128
445
FRY006 Fryns Microphthalmia Syndrome 52 0.128
446
P AST005 Asthma 76 0.128
447
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.128
448
ALK013 Alkaptonuria 58 0.128
449
c BRN108 Branchiootic Syndrome 1 63 0.128
450
ATS010 Autosomal Recessive Disease 42 0.128
451
P HRD144 Hereditary Mixed Polyposis Syndrome 54 0.128
452
P SNS001 Sensorineural Hearing Loss 59 0.128
453
GLC003 Glucose Intolerance 53 0.128
454
MCR013 Microphthalmia 60 0.128
455
PLM005 Pleomorphic Lipoma 40 0.128
456
BNR002 Bone Resorption Disease 47 0.128
457
MCR037 Macroglossia 44 0.128
458
P TRC072 Treacher Collins Syndrome 1 62 0.128
459
P PTY003 Pityriasis Rubra Pilaris 57 0.128
460
P MLN069 Melanoma, Uveal 59 0.128
461
ATH013 Atherosclerosis Susceptibility 63 0.128
462
PPL049 Papillon-Lefevre Syndrome 65 0.128
463
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.128
464
c SPL067 Split-Hand/foot Malformation 1 46 0.128
465
ORL015 Oral Squamous Cell Carcinoma 43 0.128
466
P EXN002 Exanthem 58 0.128
467
P CTN003 Cutaneous Lupus Erythematosus 52 0.128
468
DRM014 Dermatofibrosarcoma Protuberans 64 0.128
469
P KLZ004 Kala-Azar 1 41 0.128
470
P KRT028 Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant 53 0.128
471
P HYP750 Hypertriglyceridemia, Familial 62 0.128
472
APR006 Apert Syndrome 69 0.128
473
PPL052 Papillomatosis, Confluent and Reticulated 34 0.128
474
PMP006 Pemphigus Vulgaris, Familial 58 0.128
475
HSH003 Hashimoto Thyroiditis 60 0.128
476
LPM012 Lipomatosis, Multiple 60 0.128
477
c PRK082 Porokeratosis 1, Multiple Types 41 0.128
478
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.128
479
KRT019 Keratitis, Hereditary 66 0.128
480
P WHT013 White Sponge Nevus 1 44 0.128
481
P ATS364 Autism 72 0.128
482
DYS018 Dysostosis 43 0.128
483
KRT079 Keratosis Pilaris Atrophicans Faciei 27 0.128
484
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.128
485
PNC001 Pancytopenia 52 0.128
486
LPD008 Lipid Metabolism Disorder 61 0.128
487
CRB039 Cerebrovascular Disease 65 0.128
488
P CWD010 Cowden Syndrome 71 0.128
489
P BNG030 Benign Ependymoma 51 0.128
490
P BLP003 Blepharospasm 45 0.128
491
GNG006 Gingival Hypertrophy 36 0.128
492
ERY004 Erysipelas 47 0.128
493
HDR003 Hidradenitis 50 0.128
494
P PRP029 Porphyria 60 0.128
495
SKN006 Skin Sarcoidosis 42 0.128
496
GGR001 Geographic Tongue 38 0.128
497
OCL022 Ocular Melanoma 54 0.128
498
PRC013 Pericarditis 53 0.128
499
P ESP024 Esophagitis 60 0.128
500
P NPH012 Nephrotic Syndrome 62 0.128
501
HYP043 Hyperandrogenism 47 0.128
502
P HYP077 Hypertrichosis 48 0.128
503
VRR004 Verrucous Carcinoma 48 0.128
504
BLP006 Blepharoconjunctivitis 35 0.128
505
HDR002 Hidradenitis Suppurativa 54 0.128
506
c DRM040 Dermatitis Herpetiformis, Familial 35 0.128
507
KRT047 Keratosis Pilaris Atrophicans 34 0.128
508
P MYC008 Myocarditis 59 0.128
509
PRP030 Purpura 54 0.128
510
LCH003 Lichen Nitidus 30 0.128
511
P THY032 Thyroiditis 56 0.128
512
LMB050 Limbal Stem Cell Deficiency 50 0.128
513
CRV002 Cervix Uteri Carcinoma in Situ 48 0.128
514
DFF012 Differentiating Neuroblastoma 27 0.128
515
YLL002 Yellow Fever 61 0.128
516
CLF001 Cleft Lip 54 0.128
517
CLL010 Cellular Ependymoma 58 0.128
518
P ORF001 Orofaciodigital Syndrome 50 0.128
519
P DRM007 Dermatitis Herpetiformis 54 0.128
520
PRR013 Prurigo Nodularis 37 0.128
521
CRV045 Cervical Intraepithelial Neoplasia 38 0.128
522
LSH001 Leishmaniasis 63 0.128
523
P LPS004 Lupus Erythematosus 61 0.128
524
P PRD008 Periodontitis 64 0.128
525
EXP004 Exophthalmos 50 0.128
526
DCB001 Decubitus Ulcer 61 0.128
527
ESN016 Eosinophilic Pustular Folliculitis 23 0.128
528
EXG001 Exogenous Ochronosis 14 0.128
529
LCH013 Lichen Planus Pemphigoides 32 0.128
530
DMD001 Demodicidosis 23 0.128
531
GRV012 Grover's Disease 29 0.128
532
CTN007 Cutaneous Leishmaniasis 61 0.128
533
P PST059 Pustular Psoriasis 37 0.128
534
ISL121 Isolated Split Hand-Split Foot Malformation 42 0.128
535
DFF038 Diffuse Palmoplantar Keratoderma 29 0.128
536
RRG043 Rare Genetic Skin Disease 17 0.128
537
CNT114 Central Nervous System Malformation 13 0.128
538
ERY014 Erythrokeratoderma 26 0.128
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