Search results for uvs.2

308 hits were found for uvs.2

# Family MCID Name MIFTS Score
1
P UVS001 Uv-Sensitive Syndrome 39 6.525
2
c UVS003 Uv-Sensitive Syndrome 3 17 5.936
3
c UVS005 Uv-Sensitive Syndrome 1 16 5.453
4
c UVS004 Uv-Sensitive Syndrome 2 17 5.433
5
UVN001 Uv-Induced Skin Damage 20 3.564
6
MLN008 Melanoma 62 0.254
7
P CCK001 Cockayne Syndrome 61 0.210
8
DRM006 Dermatitis 66 0.117
9
SQM006 Squamous Cell Carcinoma 70 0.111
10
c BSL007 Basal Cell Carcinoma 65 0.111
11
c XRD018 Xeroderma Pigmentosum, Group a 57 0.105
12
P SKN013 Skin Benign Neoplasm 43 0.105
13
SKN016 Skin Disease 66 0.098
14
CRN024 Corneal Disease 44 0.098
15
PHT003 Phototoxic Dermatitis 35 0.098
16
CNT047 Contact Dermatitis 61 0.091
17
P PSR002 Psoriasis 61 0.091
18
EYD002 Eye Disease 61 0.091
19
P XRD010 Xeroderma Pigmentosum, Variant Type 58 0.091
20
ETH011 Ethylmalonic Encephalopathy 56 0.091
21
P KRT007 Keratoconus 48 0.091
22
SKN027 Skin Conditions 43 0.091
23
GLB003 Globe Disease 32 0.091
24
P BRS047 Breast Cancer 100 0.083
25
P ATX030 Ataxia-Telangiectasia 77 0.083
26
P LPS004 Lupus Erythematosus 64 0.083
27
P CTR002 Cataract 58 0.083
28
P ATX004 Ataxia 53 0.083
29
RTN023 Retinitis 50 0.083
30
P HPT021 Hepatitis 69 0.074
31
P HRP006 Herpes Simplex 65 0.074
32
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.074
33
BRN106 Burns 52 0.074
34
P CTN003 Cutaneous Lupus Erythematosus 48 0.074
35
SKN023 Skin Tag 44 0.074
36
AYM001 Ayme-Gripp Syndrome 41 0.074
37
NTR005 Nutritional Deficiency Disease 36 0.074
38
ALR002 Al-Raqad Syndrome 36 0.074
39
P ADN016 Adenocarcinoma 69 0.064
40
c HPT016 Hepatitis B 64 0.064
41
P CNJ013 Conjunctivitis 64 0.064
42
P RCK004 Rickets 61 0.064
43
OCL009 Ocular Cancer 59 0.064
44
ALL010 Allergic Contact Dermatitis 57 0.064
45
P TRC072 Treacher Collins Syndrome 1 52 0.064
46
KRT002 Keratomalacia 52 0.064
47
ACT008 Actinic Keratosis 51 0.064
48
PMP001 Pemphigus 50 0.064
49
P PRK001 Porokeratosis 45 0.064
50
PGM003 Pigmentation Disease 39 0.064
51
TRT001 Teratocarcinoma 38 0.064
52
P XRD027 Xeroderma Pigmentosum Group E 35 0.064
53
PHT002 Photokeratitis 31 0.064
54
CRN009 Corneal Ectasia 26 0.064
55
RCH002 Richards-Rundle Syndrome 23 0.064
56
P HYD015 Hydroa Vacciniforme 20 0.064
57
c KRT040 Keratoconus 3 14 0.064
58
HV1006 Hiv-1 80 0.052
59
P LKM002 Leukemia 71 0.052
60
KRT004 Keratitis 71 0.052
61
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.052
62
c HMP004 Hemophilia B 62 0.052
63
P ATP001 Atopic Dermatitis 62 0.052
64
SKN019 Skin Melanoma 62 0.052
65
ACN011 Acne 62 0.052
66
MTH009 Mouth Disease 61 0.052
67
BNC003 Bone Cancer 58 0.052
68
P HMP007 Hemophilia 57 0.052
69
P EXN002 Exanthem 57 0.052
70
URT039 Urticaria 57 0.052
71
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 0.052
72
P FBR017 Fibrosarcoma 56 0.052
73
PPL022 Papilloma 55 0.052
74
ERY003 Erythema Multiforme 55 0.052
75
C3D001 C3 Deficiency 53 0.052
76
P LCH002 Lichen Planus 53 0.052
77
c XRD019 Xeroderma Pigmentosum, Group C 52 0.052
78
KRT009 Keratosis 52 0.052
79
KLD001 Keloids 51 0.052
80
IMM136 Immune System Disease 51 0.052
81
c DWL002 Dowling-Degos Disease 1 49 0.052
82
LPD004 Lipoid Nephrosis 48 0.052
83
P CRN028 Corneal Ulcer 45 0.052
84
KRT008 Keratopathy 44 0.052
85
BLL004 Bullous Keratopathy 44 0.052
86
END072 Endotheliitis 42 0.052
87
c BSL024 Basal Cell Carcinoma 1 42 0.052
88
PMP004 Pemphigus Foliaceus 42 0.052
89
LCH009 Lichen Sclerosus 41 0.052
90
c PRM023 Pre-Malignant Neoplasm 41 0.052
91
CLV009 Clove Syndrome, Somatic 41 0.052
92
c CCK005 Cockayne Syndrome, Type a 39 0.052
93
c PSR017 Psoriasis 2 37 0.052
94
SNL007 Senile Cataract 37 0.052
95
DYS002 Dysplastic Nevus Syndrome 37 0.052
96
GRN007 Granuloma Annulare 37 0.052
97
CLD014 Cole Disease 37 0.052
98
BNS002 Bone Structure Disease 37 0.052
99
LNT002 Lentigo Maligna Melanoma 35 0.052
100
SKN020 Skin Papilloma 30 0.052
101
PRM243 Primary Bone Cancer 29 0.052
102
RDT005 Radiation Induced Cancer 28 0.052
103
LPD027 Lip Disease 28 0.052
104
SLR005 Solar Urticaria 27 0.052
105
FCL001 Facial Dermatosis 23 0.052
106
HYP213 Hypomelanotic Disorder 21 0.052
107
c CRB099 Cerebrooculofacioskeletal Syndrome 3 18 0.052
108
P CLR023 Colorectal Cancer 97 0.037
109
P RHM011 Rheumatoid Arthritis 89 0.037
110
c SYS001 Systemic Lupus Erythematosus 86 0.037
111
P MDL005 Medulloblastoma 77 0.037
112
ESP021 Esophageal Cancer 76 0.037
113
c CHR090 Chronic Lymphocytic Leukemia 76 0.037
114
NRL016 Neural Tube Defects 76 0.037
115
P ART022 Arthritis 75 0.037
116
P HRT032 Heart Disease 75 0.037
117
P LFR001 Li-Fraumeni Syndrome 75 0.037
118
P RTN024 Retinoblastoma 74 0.037
119
P INF038 Influenza 72 0.037
120
c FNC027 Fanconi Anemia, Complementation Group a 71 0.037
121
P NRB001 Neuroblastoma 70 0.037
122
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.037
123
TBR010 Tuberculosis 70 0.037
124
TST021 Testicular Germ Cell Tumor 69 0.037
125
P LYM118 Lymphoma 69 0.037
126
P GLB002 Glioblastoma 68 0.037
127
PCK002 Pick Disease 68 0.037
128
WRN001 Werner Syndrome 67 0.037
129
KPS004 Kaposi Sarcoma 67 0.037
130
CHG001 Chagas Disease 67 0.037
131
MLD001 Melioidosis 67 0.037
132
EWN003 Ewing Sarcoma 66 0.037
133
SMT004 Smith-Lemli-Opitz Syndrome 66 0.037
134
MYC006 Mycosis Fungoides 66 0.037
135
DWN001 Down Syndrome 66 0.037
136
SRC014 Sarcoma 66 0.037
137
ATH003 Atherosclerosis 65 0.037
138
BSL036 Basal Cell Nevus Syndrome 65 0.037
139
P AMY004 Amyloidosis 65 0.037
140
CHD001 Chediak-Higashi Syndrome 64 0.037
141
P OST002 Osteoporosis 64 0.037
142
CNN005 Connective Tissue Disease 62 0.037
143
P DRM010 Dermatomyositis 62 0.037
144
P ALP009 Alopecia Areata 62 0.037
145
LSC001 Lesch-Nyhan Syndrome 61 0.037
146
P ESP024 Esophagitis 61 0.037
147
BRS051 Breast Disease 61 0.037
148
P SYS005 Systemic Scleroderma 61 0.037
149
P NPH009 Nephrolithiasis 60 0.037
150
DRR010 Darier Disease 60 0.037
151
P GLM045 Glioma 60 0.037
152
P NRV006 Nervous System Cancer 60 0.037
153
CHL123 Chlamydia 60 0.037
154
CRV038 Cervical Squamous Cell Carcinoma 60 0.037
155
P ORL007 Oral Cavity Cancer 59 0.037
156
c HPT003 Hepatitis a 59 0.037
157
P INF032 Infertility 59 0.037
158
ALL006 Allergic Asthma 58 0.037
159
PRP030 Purpura 58 0.037
160
P GT001 Gout 58 0.037
161
P BRS044 Breast Adenocarcinoma 58 0.037
162
SCH014 Schistosomiasis 58 0.037
163
KND001 Kindler Syndrome 57 0.037
164
P CND004 Candidiasis 57 0.037
165
CTS003 Coats Disease 57 0.037
166
ALP008 Alopecia 57 0.037
167
ADM013 Adamantinoma of Long Bones 57 0.037
168
c SVR001 Severe Acute Respiratory Syndrome 57 0.037
169
ORL011 Oral Cancer 56 0.037
170
P MST009 Mastocytosis 56 0.037
171
HRP004 Herpes Zoster 56 0.037
172
NRN004 Neuroendocrine Tumor 56 0.037
173
VRL011 Viral Infectious Disease 55 0.037
174
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 55 0.037
175
P FNC043 Fanconi Anemia, Complementation Group E 55 0.037
176
MCS002 Mucositis 55 0.037
177
P RTN016 Retinal Degeneration 54 0.037
178
c PND001 Pain Disorder 54 0.037
179
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 54 0.037
180
c XRD012 Xeroderma Pigmentosum, Group D 53 0.037
181
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.037
182
ALL026 Allergic Hypersensitivity Disease 52 0.037
183
CRC006 Carcinoid Syndrome 52 0.037
184
OCL022 Ocular Melanoma 52 0.037
185
ART002 Arts Syndrome 51 0.037
186
ADN024 Adenine Phosphoribosyltransferase Deficiency 51 0.037
187
P HRD018 Hair Disease 51 0.037
188
ALL009 Allergic Conjunctivitis 51 0.037
189
BNM001 Bone Marrow Cancer 51 0.037
190
SCH002 Schnitzler Syndrome 51 0.037
191
P CTN015 Cutaneous T Cell Lymphoma 50 0.037
192
P HYP014 Hyperuricemia 50 0.037
193
c XRD013 Xeroderma Pigmentosum, Group B 50 0.037
194
EPD001 Epidermodysplasia Verruciformis 50 0.037
195
FML037 Female Breast Cancer 50 0.037
196
STM007 Stomatitis 50 0.037
197
P CLL015 Collagen Disease 50 0.037
198
c XRD015 Xeroderma Pigmentosum, Group F 49 0.037
199
CTN014 Cutaneous Mastocytosis 49 0.037
200
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.037
201
ORL005 Oral Candidiasis 48 0.037
202
ATN002 Autonomic Nervous System Disease 48 0.037
203
NPH003 Nephrocalcinosis 48 0.037
204
P TRC086 Trichohepatoenteric Syndrome 1 48 0.037
205
c XNT010 Xanthinuria, Type I 47 0.037
206
PRN014 Paronychia 47 0.037
207
PLM102 Palmoplantar Keratoderma, Epidermolytic 47 0.037
208
FLL008 Folliculitis 46 0.037
209
P FNC044 Fanconi Anemia, Complementation Group C 46 0.037
210
VCC001 Vaccinia 46 0.037
211
INC022 Inclusion-Cell Disease 46 0.037
212
PRG004 Progeria 44 0.037
213
RGH009 Right Atrial Isomerism 44 0.037
214
BNN003 Bone Inflammation Disease 44 0.037
215
APH010 Aphakia, Congenital Primary 44 0.037
216
HYP077 Hypertrichosis 44 0.037
217
RFR003 Refractive Error 43 0.037
218
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.037
219
DFF001 Diffuse Cutaneous Mastocytosis 43 0.037
220
BCK006 Back Pain 43 0.037
221
VGN023 Vaginitis 42 0.037
222
NRR001 Neuroretinitis 42 0.037
223
PTY001 Pityriasis Rosea 42 0.037
224
IMM033 Immunodeficiency Due to Purine Nucleoside Phosphorylase Deficiency 42 0.037
225
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.037
226
RPR002 Reproductive System Disease 41 0.037
227
ATS010 Autosomal Recessive Disease 41 0.037
228
MCS004 Mucosal Melanoma 41 0.037
229
NRN002 Neuronitis 41 0.037
230
SKN022 Skin Squamous Cell Carcinoma 41 0.037
231
SLF004 Sulfite Oxidase Deficiency 41 0.037
232
MLN013 Melanoma Metastasis 40 0.037
233
NSP002 Nasopharyngitis 40 0.037
234
ADT003 Auditory System Disease 40 0.037
235
PRP005 Parapsoriasis 39 0.037
236
CMM003 Common Wart 39 0.037
237
NRC019 Neurocutaneous Melanosis, Somatic 39 0.037
238
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.037
239
P VTL001 Vitelliform Macular Dystrophy 38 0.037
240
MLY001 Molybdenum Cofactor Deficiency 38 0.037
241
SPC003 Specific Developmental Disorder 38 0.037
242
P UTR038 Uterine Disease 37 0.037
243
c CHR579 Chiari Malformation Type Ii 37 0.037
244
c RBN009 Robinow Syndrome, Autosomal Recessive 37 0.037
245
URT008 Urticaria Pigmentosa 37 0.037
246
c CCK006 Cockayne Syndrome, Type B 37 0.037
247
c FNC042 Fanconi Anemia, Complementation Group D2 37 0.037
248
P XNT004 Xanthinuria 37 0.037
249
MTG002 Mutagen Sensitivity 36 0.037
250
P VTM008 Vitamin D-Dependent Rickets, Type I 36 0.037
251
GRM001 Germ Cell and Embryonal Cancer 36 0.037
252
OPT008 Optic Nerve Neoplasm 36 0.037
253
MYT011 Myotonia 36 0.037
254
ATM012 Autoimmune Disease of Blood 35 0.037
255
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.037
256
PRR013 Prurigo Nodularis 35 0.037
257
PRS025 Presbyopia 35 0.037
258
LCH003 Lichen Nitidus 34 0.037
259
PLC008 Placenta Disease 33 0.037
260
LNS003 Lens Disease 33 0.037
261
NCR002 Necrobiosis Lipoidica 32 0.037
262
c HPR001 Hprt-Related Gout 32 0.037
263
DBT007 Diabetic Cataract 32 0.037
264
P HYP612 Hypouricemia, Renal 32 0.037
265
FSR001 Fusariosis 31 0.037
266
c HYP623 Hyperuricemic Nephropathy, Familial Juvenile 1 31 0.037
267
CHR463 Chronic Actinic Dermatitis 31 0.037
268
PRN024 Purine-Pyrimidine Metabolic Disorder 31 0.037
269
VTM003 Vitamin Metabolic Disorder 30 0.037
270
MRG013 Mirage Syndrome 29 0.037
271
LCH014 Lichen Amyloidosis 29 0.037
272
PYR035 Pyrimidine Metabolic Disorder 29 0.037
273
MDD015 Mid-Dermal Elastolysis 28 0.037
274
P PHT010 Photoparoxysmal Response 1 28 0.037
275
NPH078 Nephrolithiasis, Uric Acid 28 0.037
276
c HRD142 Hereditary Xanthinuria 28 0.037
277
c XNT011 Xanthinuria, Type Ii 27 0.037
278
MRP002 Morpheaform Basal Cell Carcinoma 27 0.037
279
c CCK002 Cockayne Syndrome Type I 26 0.037
280
EXP002 Exposure Keratitis 26 0.037
281
c KRT029 Keratoconus 1 26 0.037
282
HYP649 Hyperpigmentation with or Without Hypopigmentation 25 0.037
283
ATM052 Autoimmune Disease 1 25 0.037
284
PTR001 Petrositis 24 0.037
285
PTY004 Pityriasis Lichenoides 23 0.037
286
SPR019 Superficial Keratitis 23 0.037
287
HND001 Hand Dermatosis 23 0.037
288
ATM059 Autoimmune Disease 6 22 0.037
289
ACT160 Actinic Lichen Planus 20 0.037
290
LCH008 Lichen Planus Pigmentosus 20 0.037
291
VSC009 Vascular Skin Disease 19 0.037
292
SCL001 Scalp Dermatosis 18 0.037
293
c ALP039 Alopecia Areata 1 18 0.037
294
PYR009 Pyridoxine Deficiency Anemia 18 0.037
295
c BSL028 Basal Cell Carcinoma 5 16 0.037
296
AND005 Androgen Insensitivity Syndrome, Mild 16 0.037
297
c BSL026 Basal Cell Carcinoma 3 16 0.037
298
ATM053 Autoimmune Disease 2 16 0.037
299
GLC077 Glucocorticoid Therapy, Response to 16 0.037
300
ATM054 Autoimmune Disease 3 15 0.037
301
ATM055 Autoimmune Disease 4 15 0.037
302
c KRT052 Keratoconus 6 15 0.037
303
c ALP040 Alopecia Areata 2 15 0.037
304
c KRT039 Keratoconus 2 14 0.037
305
ATM013 Autoimmune Disease of Cardiovascular System 13 0.037
306
HML018 Homologous Wasting Disease 13 0.037
307
STB001 Stable Condition Keratoconus 11 0.037
308
c ERC007 Ercc8-Related Cockayne Syndrome 11 0.037
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