Search results for "skin"

The MalaCard for "skin" has been retired.
Searching MalaCards for entries containing "skin"

5349 hits were found for 'skin'

# Family MCID Name MIFTS Score
1
c PLN018 Peeling Skin Syndrome 2 35 3.970
2
P PLN008 Peeling Skin Syndrome 47 3.673
3
SKN016 Skin Disease 68 3.598
4
c LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 38 3.248
5
P ECT007 Ectodermal Dysplasia/skin Fragility Syndrome 40 3.122
6
c PLN017 Peeling Skin Syndrome 1 33 3.106
7
c PLN021 Peeling Skin Syndrome 3 31 2.955
8
STF002 Stiff Skin Syndrome 53 2.858
9
P SKN013 Skin Benign Neoplasm 46 2.840
10
WRN004 Wrinkly Skin Syndrome 32 2.830
11
SKN023 Skin Tag 46 2.789
12
SKN024 Skin Fragility-Woolly Hair Syndrome 20 2.473
13
SKN019 Skin Melanoma 62 2.463
14
SKN002 Skin Lipoma 25 2.454
15
SKN020 Skin Papilloma 32 2.346
16
SKN018 Skin Hemangioma 40 2.315
17
RTT001 Ritter's Disease 41 2.305
18
P RST011 Restrictive Dermopathy, Lethal 38 2.305
19
GRN032 Granulomatous Slack Skin Disease 18 2.300
20
PRN056 Parana Hard-Skin Syndrome 14 2.295
21
P SKN063 Skin Creases, Congenital Symmetric Circumferential, 1 20 2.291
22
SKN022 Skin Squamous Cell Carcinoma 41 2.222
23
SKN005 Skin Atrophy 43 2.172
24
BRB006 Barber-Say Syndrome 32 2.105
25
HYP346 Hypotrichosis and Recurrent Skin Vesicles 17 2.091
26
BLL007 Bullous Skin Disease 38 1.910
27
CHR100 Chronic Ulcer of Skin 42 1.907
28
c SKN012 Skin Carcinoma in Situ 40 1.903
29
VSC012 Vesiculobullous Skin Disease 39 1.889
30
P GNR027 Generalized Peeling Skin Syndrome 22 1.885
31
SKN001 Skin Angiosarcoma 13 1.879
32
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 34 1.877
33
NDL009 Nodular Basal Cell Carcinoma 32 1.877
34
c INF144 Inflammatory Skin and Bowel Disease, Neonatal, 1 20 1.871
35
c INF146 Inflammatory Skin and Bowel Disease, Neonatal, 2 17 1.871
36
PLM082 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal 16 1.871
37
PLN020 Peeling Skin with Leukonychia, Acral Punctate Keratoses, Cheilitis, and Knuckle Pads 16 1.871
38
MLG007 Malignant Skin Fibrous Histiocytoma 31 1.863
39
SKN061 Skin Fragility-Woolly Hair-Palmoplantar Keratoderma Syndrome 10 1.863
40
SRC008 Sarcomatoid Squamous Cell Skin Carcinoma 29 1.861
41
SKN011 Skin Pilomatrix Carcinoma 21 1.861
42
SKN008 Skin Glomus Tumor 11 1.861
43
MTT001 Metatypical Basal Cell Carcinoma 16 1.858
44
EPD010 Epidermal Appendage Tumor 16 1.855
45
TNG009 Tongue Squamous Cell Carcinoma 74 1.718
46
VSC009 Vascular Skin Disease 22 1.708
47
UVN001 Uv-Induced Skin Damage 20 1.654
48
JSS001 Jessner's Lymphocytic Infiltration of the Skin 12 1.642
49
SKN027 Skin Conditions 45 1.640
50
ANG016 Angiokeratoma 38 1.638
51
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 36 1.634
52
SKN021 Skin Sarcoma 30 1.634
53
CLF045 Cleft, Median, of Upper Lip with Polyps of Facial Skin and Nasal Mucosa 19 1.630
54
P LNR015 Linear Skin Defects with Multiple Congenital Anomalies 28 1.627
55
c LNR014 Linear Skin Defects with Multiple Congenital Anomalies 3 18 1.625
56
SQM001 Squamous Cell Papilloma of Skin 14 1.625
57
CTN004 Cutaneous Fibrous Histiocytoma 42 1.623
58
VRR003 Verruciform Xanthoma of Skin 18 1.620
59
SKN010 Skin Epithelioid Hemangioma 15 1.620
60
SDD003 Saddan 30 1.617
61
P SKN009 Skin Granular Cell Tumor 16 1.617
62
DRM002 Dermoid Cyst of Skin 14 1.617
63
CLR010 Clear Cell Squamous Cell Skin Carcinoma 12 1.617
64
CTN002 Cutaneous Mucoepidermoid Carcinoma 24 1.614
65
c MLG050 Malignant Granular Cell Skin Tumor 12 1.614
66
SKN017 Skin Glomangioma 9 1.614
67
BSL002 Basaloid Squamous Cell Skin Carcinoma 7 1.614
68
ECC006 Eccrine Mixed Tumor of Skin 7 1.614
69
ACN008 Acantholytic Squamous Cell Skin Carcinoma 6 1.614
70
ADR038 Adermatoglyphia 48 1.411
71
P EHL001 Ehlers-Danlos Syndrome 61 1.393
72
KPS004 Kaposi Sarcoma 66 1.355
73
ATM016 Autoimmune Disease of Skin and Connective Tissue 31 1.353
74
SKN006 Skin Sarcoidosis 35 1.347
75
KWS001 Kwashiorkor 44 1.345
76
NRT002 Neurotic Excoriation 31 1.343
77
MLT104 Multiple Benign Circumferential Skin Creases on Limbs 19 1.339
78
P CPL006 Capillary Hemangioma 52 1.337
79
CTN013 Cutaneous Anthrax 35 1.337
80
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 35 1.334
81
P NNT037 Neonatal Inflammatory Skin and Bowel Disease 23 1.334
82
DYS044 Dysmorphism Cleft Palate Loose Skin 10 1.334
83
MCR095 Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 27 1.332
84
EYB005 Eyebrows, Duplication of, with Stretchable Skin and Syndactyly 13 1.332
85
ECC004 Eccrine Porocarcinoma 33 1.329
86
c ALB017 Albinism, Oculocutaneous, Type Vi 27 1.329
87
c SKN062 Skin Creases, Congenital Symmetric Circumferential, 2 10 1.329
88
RDS002 Red Skin Pigment Anomaly of New Guinea 6 1.329
89
CTN009 Cutaneous Adenocystic Carcinoma 32 1.326
90
c GNR024 Generalized Peeling Skin Syndrome Type C 14 1.326
91
LYM008 Lymphangiosarcoma 48 1.323
92
ECC008 Eccrine Sweat Gland Neoplasm 26 1.323
93
MNT259 Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies 14 1.323
94
SKN007 Skin Meningioma 10 1.323
95
CND003 Candidal Paronychia 10 1.323
96
PRN012 Perianal Skin Paget's Disease 7 1.323
97
SKN004 Skin Amelanotic Melanoma 6 1.323
98
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 6 1.323
99
PLN004 Plantar Verrucous Skin Carcinoma 5 1.323
100
WND001 Wound Botulism 32 1.319
101
c SPN111 Spinocerebellar Ataxia Autosomal Recessive 5 25 1.319
102
CLR015 Clear Cell Basal Cell Carcinoma 24 1.319
103
CTN010 Cutaneous Ganglioneuroma 24 1.319
104
SGN001 Signet Ring Basal Cell Carcinoma 8 1.319
105
CRS012 Carasil Syndrome 29 1.316
106
CTN001 Cutaneous Solitary Mastocytoma 28 1.316
107
ADM002 Adamantinoid Basal Cell Epithelioma 10 1.316
108
SRC003 Sarcomatoid Basal Cell Carcinoma 10 1.316
109
DRM006 Dermatitis 61 1.265
110
c BSL007 Basal Cell Carcinoma 64 1.125
111
P DWL002 Dowling-Degos Disease 1 51 1.041
112
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 58 1.035
113
P CTS001 Cutis Laxa 59 1.028
114
PGM003 Pigmentation Disease 42 1.027
115
P DRM010 Dermatomyositis 58 1.024
116
PMS001 Poems Syndrome 55 1.005
117
SBR004 Seborrheic Dermatitis 47 0.992
118
CNG008 Congenital Ichthyosiform Erythroderma 53 0.981
119
HDR004 Hidradenoma 31 0.981
120
P APL006 Aplasia Cutis Congenita 48 0.979
121
BLM001 Bloom Syndrome 62 0.973
122
P ANG013 Angioma Serpiginosum 31 0.973
123
EPD053 Epidermal Nevus, Somatic 51 0.972
124
MLT122 Multiple Self-Healing Squamous Epithelioma, Susceptiblity to 25 0.972
125
BRK001 Brooke-Spiegler Syndrome 49 0.969
126
ACR014 Acral Lentiginous Melanoma 44 0.969
127
CHN002 Chancroid 36 0.965
128
KRT013 Keratolytic Winter Erythema 24 0.965
129
MCH008 Michelin Tire Baby Syndrome 12 0.965
130
HYP691 Hypomelanosis of Ito 42 0.963
131
AML001 Amelanotic Melanoma 39 0.963
132
P SPR013 Spiradenoma 36 0.963
133
GNT020 Giant Congenital Nevus 22 0.963
134
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 35 0.961
135
P CRN038 Carney Complex Variant 51 0.958
136
NXS001 Naxos Disease 44 0.958
137
PGT003 Paget Disease, Extramammary 34 0.958
138
CTN027 Cutaneous Mastocytoma 25 0.958
139
PSD101 Pseudoxanthoma Elasticum-Like Skin Manifestations with Retinitis Pigmentosa 11 0.958
140
MCC010 Mccune-Albright Syndrome, Somatic, Mosaic 58 0.956
141
ADN015 Adenoid Basal Cell Carcinoma 36 0.956
142
c PLL014 Pellagra-Like Syndrome 17 0.956
143
DRM042 Dermatoosteolysis, Kirghizian Type 15 0.956
144
ESN002 Eosinophilia-Myalgia Syndrome 41 0.953
145
CTN012 Cutaneous Leiomyosarcoma 38 0.953
146
c GRS013 Griscelli Syndrome, Type 1 34 0.953
147
PSD059 Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency 23 0.953
148
EXF006 Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-Like 18 0.953
149
KSK002 Kosaki Overgrowth Syndrome 16 0.953
150
MCR036 Macroepiphyseal Dysplasia with Osteoporosis, Wrinkled Skin, and Aged Appearance 8 0.953
151
SPR107 Sparse Hair-Short Stature-Skin Anomalies Syndrome 8 0.953
152
P MLN043 Melanoma, Cutaneous Malignant 8 36 0.950
153
FLY003 Flynn-Aird Syndrome 16 0.950
154
EBD002 Ebd, Bart Type 12 0.950
155
P FNC043 Fanconi Anemia, Complementation Group E 45 0.947
156
NGL001 Naegeli-Franceschetti-Jadassohn Syndrome 28 0.947
157
CYS004 Cystic Basal Cell Carcinoma 27 0.947
158
MCR274 Microcephalic Primordial Dwarfism, Montreal Type 17 0.947
159
HLL006 Halal Setton Wang Syndrome 13 0.947
160
c DSP002 Dsp-Related Ectodermal Dysplasia/skin Fragility Syndrome 6 0.947
161
c PKP001 Pkp1-Related Ectodermal Dysplasia/skin Fragility Syndrome 6 0.947
162
PGM025 Pigmentation Defects-Palmoplantar Keratoderma-Skin Carcinoma Syndrome 5 0.947
163
ICH027 Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 5 0.947
164
HRD105 Hereditary Sensorimotor Neuropathy with Hyperelastic Skin 4 0.947
165
MNT019 Mental Retardation Hypotonia Skin Hyperpigmentation 3 0.947
166
SHR013 Short Stature Abnormal Skin Pigmentation Mental Retardation 3 0.947
167
MSM009 Mesomelic Dysplasia Skin Dimples 3 0.947
168
P WVR001 Weaver Syndrome 51 0.943
169
c MCL040 Macular Degeneration, Age-Related, 3 34 0.943
170
SNL003 Senile Angioma 33 0.943
171
CMB022 Combined Cellular and Humoral Immune Defects with Granulomas 29 0.943
172
PGM002 Pigmented Basal Cell Carcinoma 27 0.943
173
HDR001 Hidrocystoma 24 0.943
174
ANG065 Angioma, Tufted 22 0.943
175
ANL016 Anal Margin Carcinoma 21 0.943
176
c MLG049 Malignant Syringoma 21 0.943
177
FCL068 Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome 18 0.943
178
c MLG048 Malignant Acrospiroma 17 0.943
179
INT287 Intellectual Disability-Hypotonia-Skin Hyperpigmentation Syndrome 10 0.943
180
BRS103 Bier Spots 10 0.943
181
SKN026 Skin Cancer, Non Melanoma, Childhood 9 0.943
182
END012 Endometriosis in Scar of Skin 8 0.943
183
GLL032 Galloway-Mowat Syndrome 50 0.940
184
WDM004 Wiedemann-Steiner Syndrome 39 0.940
185
INF027 Infiltrative Basal Cell Carcinoma 27 0.940
186
SPR033 Superficial Spreading Melanoma 18 0.940
187
TNL002 Toenail Dystrophy, Isolated 18 0.940
188
CRN070 Corneodermatoosseous Syndrome 17 0.940
189
DNT019 Daentl Towsend Siegel Syndrome 14 0.940
190
NVF002 Nevi Flammei 12 0.940
191
CTN008 Cutaneous Liposarcoma 11 0.940
192
c LTH013 Lethal Restrictive Dermopathy, Lmna-Related 7 0.940
193
c LTH014 Lethal Restrictive Dermopathy, Zmpste24-Related 7 0.940
194
SBC013 Sebaceous Basal Cell Carcinoma 7 0.940
195
P APL009 Aplasia Cutis Congenita of Limbs Recessive 7 0.940
196
RYM001 Roy Maroteaux Kremp Syndrome 7 0.940
197
SQR001 Sequeiros Sack Syndrome 6 0.940
198
WDH003 Woodhouse-Sakati Syndrome 41 0.935
199
SBC009 Sebaceous Adenoma 34 0.935
200
INF028 Infundibulocystic Basal Cell Carcinoma 27 0.935
201
LMY001 Leiomyoma Cutis 25 0.935
202
ECC002 Eccrine Acrospiroma 21 0.935
203
c WVR003 Weaver Syndrome 1 21 0.935
204
CPL002 Capillary Lymphangioma 18 0.935
205
MLT066 Multiple Cutaneous and Uterine Leiomyomas 18 0.935
206
ANL007 Anal Margin Squamous Cell Carcinoma 15 0.935
207
ANL013 Anal Margin Basal Cell Carcinoma 13 0.935
208
ECC003 Eccrine Papillary Adenoma 12 0.935
209
ALG003 Al Gazali Aziz Salem Syndrome 11 0.935
210
MCR016 Micronodular Basal Cell Carcinoma 11 0.935
211
BNG008 Benign Dermal Neurilemmoma 10 0.935
212
THM006 Thumb Deformity, Alopecia, Pigmentation Anomaly 7 0.935
213
JNS005 Jones Hersh Yusk Syndrome 7 0.935
214
PLM113 Palmoplantar Keratoderma-Sclerodactyly Syndrome 7 0.935
215
HRY007 Hairy Palms and Soles 7 0.935
216
TNG005 Tang Hsi Ryu Syndrome 6 0.935
217
DRM001 Dermal Unilateral Segmental Cavernous Angioma 6 0.935
218
MST010 Mastocytosis Cutaneous with Short Stature Conductive Hearing Loss and Microtia 6 0.935
219
GRB001 Grubben De Cock Borghgraef Syndrome 6 0.935
220
JDG001 Judge Misch Wright Syndrome 5 0.935
221
BDH001 Boudhina Yedes Khiari Syndrome 4 0.935
222
MLN017 Milner Khallouf Gibson Syndrome 4 0.935
223
RVL001 Ruvalcaba Churesigaew Myhre Syndrome 4 0.935
224
ELL003 Elliott Ludman Teebi Syndrome 4 0.935
225
ANG030 Angiomatosis, Diffuse Corticomeningeal, of Divry and Van Bogaert 4 0.935
226
MGR004 Megarbane Jalkh Syndrome 4 0.935
227
P ATP001 Atopic Dermatitis 62 0.145
228
P PSR002 Psoriasis 63 0.139
229
BRN106 Burns 52 0.119
230
CTN007 Cutaneous Leishmaniasis 62 0.112
231
P LYM118 Lymphoma 70 0.111
232
ADM013 Adamantinoma of Long Bones 59 0.110
233
KRT009 Keratosis 50 0.094
234
ACN011 Acne 63 0.091
235
ACT008 Actinic Keratosis 53 0.090
236
AYM001 Ayme-Gripp Syndrome 45 0.087
237
EPD016 Epidermolysis Bullosa 57 0.086
238
ALL026 Allergic Hypersensitivity Disease 53 0.084
239
ATP002 Atopy 63 0.083
240
CNT047 Contact Dermatitis 62 0.082
241
P LPS004 Lupus Erythematosus 63 0.081
242
URT039 Urticaria 59 0.079
243
MYC006 Mycosis Fungoides 66 0.079
244
PRM025 Primary Bacterial Infectious Disease 43 0.079
245
WRN005 Wrinkles 37 0.076
246
PMP001 Pemphigus 49 0.074
247
TBR010 Tuberculosis 69 0.073
248
MLG108 Malignant Melanoma, Somatic 67 0.073
249
CLL003 Cellulitis 49 0.073
250
CNN005 Connective Tissue Disease 61 0.070
251
P ART022 Arthritis 75 0.070
252
P EXN002 Exanthem 57 0.070
253
P NRP001 Neuropathy 60 0.070
254
P LPR003 Leprosy 68 0.069
255
P LKM002 Leukemia 70 0.069
256
BLL006 Bullous Pemphigoid 58 0.067
257
RSC001 Rosacea 53 0.067
258
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.066
259
END072 Endotheliitis 42 0.066
260
ALL010 Allergic Contact Dermatitis 57 0.065
261
EPD001 Epidermodysplasia Verruciformis 50 0.063
262
P PSD087 Pseudoxanthoma Elasticum 67 0.063
263
P BRS047 Breast Cancer 100 0.062
264
IMP004 Impetigo 42 0.062
265
PPL022 Papilloma 55 0.061
266
P CTN015 Cutaneous T Cell Lymphoma 50 0.060
267
BRN105 Burn Scar 37 0.060
268
PLM102 Palmoplantar Keratoderma, Epidermolytic 48 0.059
269
MRK001 Merkel Cell Carcinoma 51 0.057
270
CLV009 Clove Syndrome, Somatic 42 0.057
271
FCL001 Facial Dermatosis 25 0.057
272
P DRM007 Dermatitis Herpetiformis 46 0.056
273
P KRT005 Keratoacanthoma 45 0.056
274
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.055
275
MCR013 Microphthalmia 59 0.055
276
C3D001 C3 Deficiency 53 0.055
277
IMM136 Immune System Disease 50 0.055
278
SRC014 Sarcoma 66 0.054
279
P SYS005 Systemic Scleroderma 58 0.054
280
ALP008 Alopecia 55 0.054
281
KLD001 Keloids 51 0.054
282
c LCL006 Localized Scleroderma 59 0.053
283
P NRV006 Nervous System Cancer 62 0.053
284
NTH001 Netherton Syndrome 52 0.053
285
P AST005 Asthma 82 0.052
286
P PLY019 Polyneuropathy 54 0.052
287
LYM006 Lymphoepithelioma-Like Carcinoma 42 0.052
288
PSR001 Psoriatic Arthritis 64 0.051
289
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 54 0.051
290
c BSL024 Basal Cell Carcinoma 1 45 0.051
291
P PMP005 Pemphigus Vulgaris 43 0.051
292
P HMN010 Hemangioma 60 0.050
293
P THY032 Thyroiditis 54 0.050
294
DBT062 Diabetic Foot Ulcers 52 0.050
295
PYD002 Pyoderma 49 0.050
296
HYP457 Hypertrophic Scars 45 0.050
297
c BSL025 Basal Cell Carcinoma 2 19 0.050
298
P INF032 Infertility 61 0.050
299
P CTN003 Cutaneous Lupus Erythematosus 50 0.050
300
EPD006 Epidermolysis Bullosa Acquisita 45 0.050
301
c SYS001 Systemic Lupus Erythematosus 87 0.049
302
P HRP006 Herpes Simplex 65 0.049
303
P RHN004 Rhinitis 61 0.049
304
INC021 Incontinentia Pigmenti 60 0.049
305
c PND001 Pain Disorder 55 0.049
306
CRC006 Carcinoid Syndrome 51 0.049
307
KND001 Kindler Syndrome 50 0.049
308
SCB001 Scabies 45 0.049
309
VSC011 Vasculitis 62 0.049
310
DRM014 Dermatofibrosarcoma Protuberans 60 0.049
311
PYD001 Pyoderma Gangrenosum 49 0.049
312
ECT006 Ectodermal Dysplasia 47 0.049
313
IRR003 Irritant Dermatitis 46 0.049
314
c PRM023 Pre-Malignant Neoplasm 43 0.049
315
c CHR579 Chiari Malformation Type Ii 38 0.049
316
P MDL005 Medulloblastoma 77 0.048
317
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.048
318
P HPT021 Hepatitis 70 0.047
319
LSH001 Leishmaniasis 62 0.047
320
NRN004 Neuroendocrine Tumor 54 0.047
321
P MST009 Mastocytosis 54 0.047
322
P BCL006 B-Cell Lymphomas 64 0.046
323
EWN003 Ewing Sarcoma 64 0.046
324
ERY003 Erythema Multiforme 57 0.046
325
P OBS005 Obesity 93 0.046
326
P PNM007 Pneumonia 66 0.046
327
P PRP003 Porphyria Cutanea Tarda 64 0.046
328
CTS003 Coats Disease 57 0.046
329
WLL006 Wells Syndrome 56 0.046
330
DCB001 Decubitus Ulcer 44 0.046
331
MLL001 Molluscum Contagiosum 41 0.046
332
GRM001 Germ Cell and Embryonal Cancer 39 0.046
333
c DRM035 Dermatitis, Atopic 2 30 0.046
334
LGD001 Leg Dermatosis 19 0.046
335
TST021 Testicular Germ Cell Tumor 70 0.045
336
OCL009 Ocular Cancer 62 0.045
337
PRP030 Purpura 59 0.045
338
P NLD001 Nail Disease 56 0.045
339
ACR041 Acromelic Frontonasal Dysostosis 46 0.045
340
DSC009 Discoid Lupus Erythematosus 44 0.045
341
P CLR023 Colorectal Cancer 97 0.044
342
ALL003 Allergic Rhinitis 64 0.044
343
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 52 0.044
344
BSC001 Buschke-Ollendorff Syndrome 49 0.044
345
c CLL013 Cell Type Cancer 48 0.044
346
ALR002 Al-Raqad Syndrome 36 0.044
347
P ADN016 Adenocarcinoma 69 0.044
348
CHL071 Child Syndrome 58 0.044
349
FCL009 Focal Dermal Hypoplasia 54 0.044
350
P SYP003 Syphilis 53 0.044
351
P PRK001 Porokeratosis 44 0.044
352
NRN002 Neuronitis 42 0.044
353
BRS090 Breast Reconstruction 39 0.044
354
PMP004 Pemphigus Foliaceus 39 0.044
355
PHT003 Phototoxic Dermatitis 38 0.044
356
GRN007 Granuloma Annulare 35 0.044
357
ULC005 Ulcer of Lower Limbs 22 0.044
358
P ESN007 Eosinophilia 61 0.043
359
P ALP009 Alopecia Areata 61 0.043
360
ERY021 Erythrokeratodermia Variabilis Et Progressiva 48 0.043
361
ECT005 Ectropion 40 0.043
362
P HYP040 Hypospadias 57 0.042
363
P EPD003 Epidermolysis Bullosa Simplex 51 0.042
364
DRM011 Dermatophytosis 45 0.042
365
CLC001 Calciphylaxis 40 0.042
366
P SYR003 Syringoma 38 0.042
367
PCK002 Pick Disease 67 0.041
368
P XRD010 Xeroderma Pigmentosum, Variant Type 58 0.041
369
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.041
370
HDR003 Hidradenitis 46 0.041
371
MYC019 Mycobacterium Marinum 28 0.041
372
P ICH023 Ichthyosis, Acquired 20 0.041
373
DBT010 Diabetic Neuropathy 55 0.041
374
KDS001 Kid Syndrome 53 0.041
375
P ICH001 Ichthyosis Vulgaris 44 0.041
376
BLL012 Bullous Impetigo 35 0.041
377
c RNL016 Renal Infectious Disease 24 0.041
378
P DYS007 Dyskeratosis Congenita 63 0.040
379
P PRP029 Porphyria 58 0.040
380
ABL002 Ablepharon-Macrostomia Syndrome 57 0.040
381
P LCH002 Lichen Planus 53 0.040
382
CDS001 Cadasil 50 0.040
383
FLL008 Folliculitis 47 0.040
384
BRT030 Birth Defects 43 0.040
385
c ATP016 Atopic Dermatitis 3 18 0.040
386
P ANP001 Anaplastic Large Cell Lymphoma 58 0.039
387
P SML001 Small Cell Carcinoma 57 0.039
388
P HST010 Histiocytosis 55 0.039
389
HLY001 Hailey-Hailey Disease 53 0.039
390
PRT011 Protein C Deficiency 51 0.039
391
P OCL002 Oculocutaneous Albinism 51 0.039
392
c ATP017 Atopic Dermatitis 4 18 0.039
393
c ATP018 Atopic Dermatitis 5 17 0.039
394
P RHM011 Rheumatoid Arthritis 88 0.038
395
P RTH001 Rothmund-Thomson Syndrome 57 0.038
396
ACN002 Acanthosis Nigricans 57 0.038
397
PRS047 Prostatitis 56 0.038
398
P EHL033 Ehlers-Danlos Syndrome, Classic Type 54 0.038
399
VND001 Vein Disease 52 0.038
400
LPR001 Lepromatous Leprosy 49 0.038
401
URB001 Urbach-Wiethe Disease 48 0.038
402
VCC001 Vaccinia 46 0.038
403
ACN018 Acne Inversa, Familial, 1 45 0.038
404
URT001 Urethritis 40 0.038
405
ERY017 Erythema Elevatum Diutinum 39 0.038
406
TNP001 Tinea Pedis 39 0.038
407
HND001 Hand Dermatosis 25 0.038
408
c BSL026 Basal Cell Carcinoma 3 19 0.038
409
c LPN003 Lipn-Related Autosomal Recessive Congenital Ichthyosis 10 0.038
410
c ABC002 Abca12-Related Autosomal Recessive Congenital Ichthyosis 8 0.038
411
c CYP003 Cyp4f22-Related Autosomal Recessive Congenital Ichthyosis 7 0.038
412
c ALX004 Alox12b-Related Autosomal Recessive Congenital Ichthyosis 7 0.038
413
c ALX005 Aloxe3-Related Autosomal Recessive Congenital Ichthyosis 7 0.038
414
c PNP002 Pnpla1-Related Autosomal Recessive Congenital Ichthyosis 7 0.038
415
c TGM001 Tgm1-Related Autosomal Recessive Congenital Ichthyosis 7 0.038
416
VSC007 Vascular Disease 67 0.037
417
BRS051 Breast Disease 62 0.037
418
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.037
419
P VNS003 Venous Insufficiency 53 0.037
420
HYP077 Hypertrichosis 52 0.037
421
NSD001 Nose Disease 52 0.037
422
PNN001 Panniculitis 50 0.037
423
LYM024 Lymphatic System Disease 50 0.037
424
P EPD002 Epidermolytic Hyperkeratosis 49 0.037
425
PLL012 Pollen Allergy 45 0.037
426
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.037
427
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.037
428
LYM052 Lymphomatoid Papulosis 41 0.037
429
PTY001 Pityriasis Rosea 41 0.037
430
YWS001 Yaws 41 0.037
431
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.037
432
c PSR017 Psoriasis 2 32 0.037
433
RDT005 Radiation Induced Cancer 28 0.037
434
ISC004 Ischemia 59 0.037
435
VRR004 Verrucous Carcinoma 53 0.037
436
ADL002 Adult Syndrome 53 0.037
437
SML033 Small Cell Cancer of the Lung, Somatic 53 0.037
438
SZR001 Sezary's Disease 53 0.037
439
PTY003 Pityriasis Rubra Pilaris 46 0.037
440
IMM127 Immune System Cancer 42 0.037
441
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 37 0.037
442
GLB003 Globe Disease 35 0.037
443
c SCL052 Scleroderma, Familial Progressive 27 0.037
444
ICH031 Ichthyosis with Confetti 26 0.037
445
c ADL017 Adult T-Cell Leukemia 58 0.036
446
HRP004 Herpes Zoster 56 0.036
447
P EPD009 Epidermolysis Bullosa Dystrophica 54 0.036
448
P HRD018 Hair Disease 50 0.036
449
HDN002 Head Injury 45 0.036
450
URT008 Urticaria Pigmentosa 38 0.036
451
SBC017 Sebaceous Gland Disease 36 0.036
452
ACR005 Acrodermatitis 34 0.036
453
NCR002 Necrobiosis Lipoidica 30 0.036
454
SCL022 Scleredema 25 0.036
455
c ICH042 Ichthyosis, Congenital, Autosomal Recessive 6 25 0.036
456
c ICH040 Ichthyosis, Congenital, Autosomal Recessive 4a 25 0.036
457
c ICH038 Ichthyosis, Congenital, Autosomal Recessive 3 25 0.036
458
c ICH050 Ichthyosis, Congenital, Autosomal Recessive 5 24 0.036
459
c ICH044 Ichthyosis, Congenital, Autosomal Recessive 8 23 0.036
460
c ICH039 Ichthyosis, Congenital, Autosomal Recessive 10 22 0.036
461
c ICH048 Ichthyosis, Congenital, Autosomal Recessive 9 21 0.036
462
PRP027 Peripheral Vascular Disease 69 0.035
463
LYM115 Lymphoma, Non-Hodgkin 65 0.035
464
BSL036 Basal Cell Nevus Syndrome 65 0.035
465
TBR024 Tuberous Sclerosis-1 65 0.035
466
MTH009 Mouth Disease 63 0.035
467
HTC002 Hutchinson-Gilford Progeria 62 0.035
468
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.035
469
ALL006 Allergic Asthma 58 0.035
470
PBL001 Piebaldism 57 0.035
471
ORL011 Oral Cancer 55 0.035
472
FDL002 Food Allergy 54 0.035
473
P LYM033 Lymphoproliferative Syndrome 53 0.035
474
PRT014 Protein S Deficiency 52 0.035
475
P LTR001 Lateral Sclerosis 52 0.035
476
P TCL004 T-Cell Leukemia 46 0.035
477
EPD028 Epidermolysis Bullosa Simplex, Dowling-Meara Type 44 0.035
478
ANH002 Anhidrosis 42 0.035
479
P PRP034 Purpura Fulminans 42 0.035
480
c EHL054 Ehlers-Danlos Syndrome, Type Vi 42 0.035
481
EPD062 Epidermolysis Bullosa, Junctional, Non-Herlitz Type 41 0.035
482
TRC010 Trichotillomania 41 0.035
483
ERY004 Erysipelas 40 0.035
484
PRL019 Prolidase Deficiency 38 0.035
485
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 36 0.035
486
NTR042 Neutrophilic Dermatosis, Acute Febrile 30 0.035
487
ACR034 Acrogeria, Gottron Type 26 0.035
488
c CTS019 Cutis Laxa, Ad 26 0.035
489
P AMY004 Amyloidosis 64 0.034
490
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.034
491
ANG020 Angiosarcoma 52 0.034
492
CHC001 Chickenpox 52 0.034
493
CCT002 Cicatricial Pemphigoid 51 0.034
494
HYP542 Hypersensitivity Syndrome, Carbamazepine-Induced 50 0.034
495
MLK003 Melkersson-Rosenthal Syndrome 50 0.034
496
c EHL055 Ehlers-Danlos Syndrome, Type Iii 50 0.034
497
P CLL015 Collagen Disease 49 0.034
498
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.034
499
FBR003 Fibrous Histiocytoma 42 0.034
500
BLD054 Blood Protein Disease 40 0.034
501
TNC003 Tinea Corporis 38 0.034
502
c ICH041 Ichthyosis, Autosomal Recessive 4b 35 0.034
503
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.034
504
URT037 Urethral Stricture 33 0.034
505
CTS011 Cutis Marmorata Telangiectatica Congenita 30 0.034
506
MLR001 Miliaria Rubra 25 0.034
507
HYP213 Hypomelanotic Disorder 21 0.034
508
c BSL028 Basal Cell Carcinoma 5 19 0.034
509
ADR007 Adrenoleukodystrophy 71 0.033
510
c HPT001 Hepatitis C 68 0.033
511
WRN001 Werner Syndrome 67 0.033
512
P MYP004 Myopathy 67 0.033
513
P LYM025 Lymphedema 61 0.033
514
DRR010 Darier Disease 61 0.033
515
P MRT001 Muir-Torre Syndrome 58 0.033
516
NRM005 Neuromuscular Disease 57 0.033
517
P PRP019 Peripheral Nervous System Disease 54 0.033
518
P ACT135 Acute Graft Versus Host Disease 53 0.033
519
LYM019 Lymphosarcoma 53 0.033
520
c CHR417 Chronic Graft Versus Host Disease 50 0.033
521
ACR003 Acrodermatitis Enteropathica 48 0.033
522
HST009 Histiocytoma 47 0.033
523
c ALB021 Albinism, Oculocutaneous, Type Ii 46 0.033
524
PHY002 Physical Disorder 44 0.033
525
ALB002 Albinism 43 0.033
526
CMP010 Complex Regional Pain Syndrome 42 0.033
527
c SCN006 Secondary Syphilis 41 0.033
528
DFF003 Diffuse Scleroderma 41 0.033
529
RDN001 Reading Disorder 39 0.033
530
ART006 Arthus Reaction 38 0.033
531
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 33 0.033
532
c TRC078 Trichohepatoenteric Syndrome 2 31 0.033
533
ANG061 Angular Cheilitis 31 0.033
534
MLR009 Miliaria 30 0.033
535
c BSL011 Basal Cell Carcinoma, Multiple 27 0.033
536
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.033
537
ERY010 Erythrasma 19 0.033
538
c ICH045 Ichthyosis, Congenital, Autosomal Recessive 7 16 0.033
539
c BCT003 Bacterial Exanthem 14 0.033
540
P RNL014 Renal Cell Carcinoma 81 0.032
541
FBR012 Fabry Disease 69 0.032
542
CST001 Costello Syndrome 69 0.032
543
LYM017 Lyme Disease 63 0.032
544
MNK001 Menkes Disease 61 0.032
545
P CCK001 Cockayne Syndrome 59 0.032
546
c SYS004 Systemic Mastocytosis 59 0.032
547
P RBL001 Rubella 56 0.032
548
ONC002 Onchocerciasis 50 0.032
549
MND007 Mandibuloacral Dysplasia 49 0.032
550
ICH054 Ichthyosis, X-Linked 48 0.032
551
LPD004 Lipoid Nephrosis 48 0.032
552
c PSR021 Psoriasis 14, Pustular 47 0.032
553
c EHL032 Ehlers-Danlos Syndrome, Type Viib 47 0.032
554
FSC004 Fasciitis 46 0.032
555
c CHR431 Chronic Venous Insufficiency 44 0.032
556
LCH009 Lichen Sclerosus 42 0.032
557
STT007 Steatocystoma Multiplex 42 0.032
558
CHR031 Chromoblastomycosis 42 0.032
559
c ADL001 Adult Lymphoma 41 0.032
560
PRP005 Parapsoriasis 39 0.032
561
HYL004 Hyaline Fibromatosis Syndrome 39 0.032
562
PRN049 Paraneoplastic Pemphigus 39 0.032
563
CRB009 Cerebritis 38 0.032
564
EPD022 Epidermolysis Bullosa Pruriginosa 38 0.032
565
CHR415 Chronic Venous Leg Ulcers 38 0.032
566
LCH011 Lichen Planopilaris 37 0.032
567
EPD061 Epidermolysis Bullosa, Junctional, Herlitz Type 36 0.032
568
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 31 0.032
569
SCR033 Scar Contracture 26 0.032
570
c CTS031 Cutis Laxa, Autosomal Dominant 2 22 0.032
571
HRD113 Hereditary Acrokeratotic Poikiloderma, Weary Type 13 0.032
572
P MLT019 Multiple Myeloma 80 0.031
573
P NRV007 Nervous System Disease 71 0.031
574
P MSC005 Muscular Dystrophy 64 0.031
575
CHR063 Chronic Mucocutaneous Candidiasis 61 0.031
576
RHM027 Rheumatic Disease 57 0.031
577
BLS001 Blau Syndrome 56 0.031
578
ORL015 Oral Squamous Cell Carcinoma 56 0.031
579
VSC006 Vascular Cancer 54 0.031
580
P SPS003 Spastic Diplegia 53 0.031
581
P END033 Endocarditis 52 0.031
582
CLN019 Colonic Disease 50 0.031
583
RYN003 Reynolds Syndrome 49 0.031
584
ECZ002 Eczema Herpeticum 46 0.031
585
CLR065 Colorectal Adenomatous Polyposis, Autosomal Recessive, with Pilomatricomas 46 0.031
586
EYL005 Eyelid Disease 42 0.031
587
ADN002 Adenoiditis 40 0.031
588
GRV012 Grover's Disease 38 0.031
589
ELP001 Elephantiasis 36 0.031
590
INT221 Intravascular Large B-Cell Lymphoma 36 0.031
591
PRS063 Paresthesia 36 0.031
592
ENT005 Entropion 32 0.031
593
c EHL027 Ehlers-Danlos Syndrome, Type Viic 32 0.031
594
c AST037 Asthma 1 31 0.031
595
ACR097 Acrodermatitis Chronica Atrophicans 26 0.031
596
c CTS037 Cutis Laxa, Autosomal Recessive, Type Ib 20 0.031
597
ANX002 Anxiety Disorder 69 0.030
598
P KDN017 Kidney Cancer 67 0.030
599
P CRD013 Cardiofaciocutaneous Syndrome 63 0.030
600
P ART023 Arthropathy 63 0.030
601
BRN024 Bronchitis 63 0.030
602
OMN001 Omenn Syndrome 61 0.030
603
LYM021 Lymphadenitis 58 0.030
604
P ORL007 Oral Cavity Cancer 58 0.030
605
P MCR129 Microvascular Complications of Diabetes 1 57 0.030
606
SPT005 Spotted Fever 56 0.030
607
PLS011 Plasmacytoma 56 0.030
608
RCT018 Rectal Neoplasm 55 0.030
609
SML019 Smallpox 53 0.030
610
NPH018 Nephrogenic Systemic Fibrosis 51 0.030
611
HND002 Hand, Foot and Mouth Disease 48 0.030
612
YLL001 Yellow Nail Syndrome 47 0.030
613
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.030
614
MLT016 Multicentric Reticulohistiocytosis 46 0.030
615
LMT001 Limited Scleroderma 45 0.030
616
GDS001 Good Syndrome 45 0.030
617
P PLL002 Pellagra 45 0.030
618
ATN004 Autonomic Neuropathy 44 0.030
619
c XRD015 Xeroderma Pigmentosum, Group F 44 0.030
620
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 42 0.030
621
c ALB009 Albinism, Oculocutaneous, Type Ia 41 0.030
622
PYG006 Pyogenic Granuloma 41 0.030
623
CLD014 Cole Disease 39 0.030
624
P EHL043 Ehlers-Danlos Syndrome, Progeroid Type, 1 38 0.030
625
P PHT010 Photoparoxysmal Response 1 37 0.030
626
BZX001 Bazex Syndrome 37 0.030
627
PLC008 Placenta Disease 36 0.030
628
LYM023 Lymphatic System Cancer 35 0.030
629
EPD056 Epidermolysis Bullosa Simplex-Mp 33 0.030
630
HRZ001 Huriez Syndrome 33 0.030
631
c CLR079 Colorectal Cancer 2 31 0.030
632
CYL004 Cylindromatosis, Familial 29 0.030
633
ATM052 Autoimmune Disease 1 28 0.030
634
MLD003 Meleda Disease 26 0.030
635
TRN023 Transient Bullous of the Newborn 25 0.030
636
SLR005 Solar Urticaria 24 0.030
637
FCL045 Focal Facial Dermal Dysplasia 3, Setleis Type 22 0.030
638
c PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 18 0.030
639
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.029
640
P THR014 Thrombocytopenia 64 0.029
641
P NMN002 Niemann-Pick Disease 63 0.029
642
P SNS014 Sinusitis 60 0.029
643
VRL011 Viral Infectious Disease 59 0.029
644
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 58 0.029
645
BTN003 Biotinidase Deficiency 56 0.029
646
HYP266 Hypoxia 55 0.029
647
HDN004 Head and Neck Carcinoma 55 0.029
648
END030 End Stage Renal Failure 52 0.029
649
TLN003 Telangiectasis 52 0.029
650
MST017 Mast Cell Disease 52 0.029
651
ART001 Arterial Tortuosity Syndrome 52 0.029
652
P FML012 Familial Partial Lipodystrophy 51 0.029
653
INT253 Intestinal Benign Neoplasm 50 0.029
654
P CHR345 Chronic Pain 49 0.029
655
RFL001 Reflex Sympathetic Dystrophy 48 0.029
656
PST062 Pustulosis Palmaris Et Plantaris 47 0.029
657
PPL049 Papillon-Lefevre Syndrome 46 0.029
658
PRP082 Porphyria, Congenital Erythropoietic 46 0.029
659
ALN001 Aland Island Eye Disease 45 0.029
660
DBT008 Diabetic Angiopathy 45 0.029
661
ECT078 Ectodermal Dysplasia 2, Clouston Type 45 0.029
662
CRN024 Corneal Disease 44 0.029
663
EPD047 Epidermolysis Bullosa Simplex, Koebner Type 42 0.029
664
PST053 Postherpetic Neuralgia 41 0.029
665
HMT018 Hematopoietic Stem Cell Transplantation 41 0.029
666
WTH001 Withdrawal Disorder 41 0.029
667
SBC012 Subcorneal Pustular Dermatosis 39 0.029
668
RCT017 Rectal Disease 39 0.029
669
ADJ001 Adjustment Disorder 38 0.029
670
EPD045 Epidermolysis Bullosa, Junctional, with Pyloric Stenosis 37 0.029
671
IMP003 Impaired Renal Function Disease 37 0.029
672
c CCK006 Cockayne Syndrome, Type B 37 0.029
673
MSC004 Muscle Tissue Disease 36 0.029
674
MLG088 Malignant Germ Cell Tumor 36 0.029
675
SPR005 Superficial Basal Cell Carcinoma 34 0.029
676
CHR463 Chronic Actinic Dermatitis 33 0.029
677
EHL060 Ehlers-Danlos Syndrome Due to Tenascin X Deficiency 30 0.029
678
PMP009 Pemphigus Erythematosus 29 0.029
679
ERY001 Erysipeloid 28 0.029
680
OCL034 Oculocerebrocutaneous Syndrome 28 0.029
681
c ICH051 Ichthyosis, Congenital, Autosomal Recessive 11 27 0.029
682
GRD005 Geroderma Osteodysplasticum 25 0.029
683
EPD031 Epidermolysis Bullosa Simplex, Ogna Type 22 0.029
684
c BSL029 Basal Cell Carcinoma 6 19 0.029
685
c BSL027 Basal Cell Carcinoma 4 18 0.029
686
c ATP019 Atopic Dermatitis 6 17 0.029
687
c ATP021 Atopic Dermatitis 8 16 0.029
688
P OST012 Osteoarthritis 82 0.028
689
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.028
690
P ATX030 Ataxia-Telangiectasia 76 0.028
691
P HRT032 Heart Disease 76 0.028
692
c CHR090 Chronic Lymphocytic Leukemia 74 0.028
693
GST019 Gastrointestinal Stromal Tumor 72 0.028
694
KWS002 Kawasaki Disease 70 0.028
695
P ALP004 Alport Syndrome 68 0.028
696
P CWD006 Cowden Syndrome 1 68 0.028
697
PLM001 Pulmonary Tuberculosis 68 0.028
698
P OST005 Osteogenesis Imperfecta 67 0.028
699
P CNJ013 Conjunctivitis 65 0.028
700
MSL001 Measles 61 0.028
701
P GST049 Gastrointestinal System Cancer 60 0.028
702
CRV038 Cervical Squamous Cell Carcinoma 59 0.028
703
ADN018 Adenoma 59 0.028
704
P FCS002 Fucosidosis 57 0.028
705
P GRS014 Griscelli Syndrome, Type 2 55 0.028
706
NRF007 Neurofibroma 52 0.028
707
P HYP098 Hypereosinophilic Syndrome 51 0.028
708
PRP021 Peripheral Nervous System Neoplasm 50 0.028
709
CSY001 C Syndrome 49 0.028
710
BCT015 Bacteremia 48 0.028
711
XNT003 Xanthomatosis 47 0.028
712
P HYP087 Hypotrichosis 45 0.028
713
TBR006 Tuberculoid Leprosy 44 0.028
714
VHW001 Vohwinkel Syndrome 41 0.028
715
MYC013 Mycobacterium Abscessus 40 0.028
716
c CCK005 Cockayne Syndrome, Type a 39 0.028
717
PRR013 Prurigo Nodularis 37 0.028
718
SWT003 Sweat Gland Disease 37 0.028
719
LPD014 Lipodermatosclerosis 36 0.028
720
ALL007 Allergic Urticaria 34 0.028
721
c EHL028 Ehlers-Danlos Syndrome, Type Viii 34 0.028
722
MJD001 Majeed Syndrome 33 0.028
723
OCC001 Occupational Dermatitis 33 0.028
724
MYC014 Mycobacterium Chelonae 32 0.028
725
BWN006 Bowen's Disease 31 0.028
726
c AST039 Asthma 2 31 0.028
727
EPD040 Epidermolysis Bullosa Simplex with Pyloric Atresia 29 0.028
728
ESN016 Eosinophilic Pustular Folliculitis 28 0.028
729
P MLT048 Multiple Familial Trichoepithelioma 27 0.028
730
c KRT055 Keratoderma, Palmoplantar, Punctate Type Ia 25 0.028
731
HYP160 Hyperkeratosis Lenticularis Perstans 23 0.028
732
SCL001 Scalp Dermatosis 20 0.028
733
FCL067 Focal Facial Dermal Dysplasia 1, Brauer Type 19 0.028
734
RMB001 Rombo Syndrome 18 0.028
735
c EFM001 Efemp2-Related Cutis Laxa 17 0.028
736
c FBL003 Fbln5-Related Cutis Laxa 16 0.028
737
c ALD008 Aldh18a1-Related Cutis Laxa 15 0.028
738
c LTB003 Ltbp4-Related Cutis Laxa 14 0.028
739
c PYC002 Pycr1-Related Cutis Laxa 12 0.028
740
c ELN002 Eln-Related Cutis Laxa 8 0.028
741
P PNC035 Pancreatic Cancer 85 0.026
742
MRF001 Marfan Syndrome 73 0.026
743
c HPT073 Hepatitis C Virus 72 0.026
744
c NRF018 Neurofibromatosis, Type 1 68 0.026
745
SVR004 Severe Combined Immunodeficiency 68 0.026
746
SMT004 Smith-Lemli-Opitz Syndrome 67 0.026
747
CHR012 Chronic Granulomatous Disease 65 0.026
748
BRC012 Brucellosis 65 0.026
749
MCK007 Muckle-Wells Syndrome 61 0.026
750
BHC003 Behcet Syndrome 61 0.026
751
P MCP010 Mucopolysaccharidosis 58 0.026
752
ADL030 Adult-Onset Still's Disease 57 0.026
753
JNT002 Joint Disorders 56 0.026
754
RBS003 Rabson-Mendenhall Syndrome 55 0.026
755
PRC002 Paracoccidioidomycosis 55 0.026
756
HST011 Histoplasmosis 54 0.026
757
P ATX004 Ataxia 53 0.026
758
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 51 0.026
759
OCL022 Ocular Melanoma 51 0.026
760
P WRD020 Waardenburg Syndrome, Type 4a 50 0.026
761
ACD009 Acid-Labile Subunit, Deficiency of 48 0.026
762
LKC003 Leukocyte Disease 47 0.026
763
CRY004 Cryoglobulinemia 47 0.026
764
HPR003 Heparin-Induced Thrombocytopenia 46 0.026
765
VSC047 Vascular Malformation 45 0.026
766
PRP036 Peripheral T-Cell Lymphoma 45 0.026
767
P CRV039 Cervicitis 44 0.026
768
FBR054 Fibroma 43 0.026
769
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 42 0.026
770
c CLR085 Colorectal Cancer 1 42 0.026
771
BCK006 Back Pain 42 0.026
772
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.026
773
DFF001 Diffuse Cutaneous Mastocytosis 41 0.026
774
CHL028 Childhood Type Dermatomyositis 40 0.026
775
NTR005 Nutritional Deficiency Disease 39 0.026
776
CRC001 Cercarial Dermatitis 37 0.026
777
MCR103 Microtia 37 0.026
778
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 36 0.026
779
c CNN010 Connective Tissue Benign Neoplasm 35 0.026
780
ADN013 Adenoid Squamous Cell Carcinoma 35 0.026
781
ANG037 Angiomatosis 34 0.026
782
FLL019 Follicular Mucinosis 34 0.026
783
NVS007 Nevus of Ota 33 0.026
784
EPD033 Epidermolysis Bullosa, Lethal Acantholytic 33 0.026
785
OCH001 Ochronosis 32 0.026
786
TNC001 Tinea Cruris 31 0.026
787
XRD026 Xeroderma Pigmentosum-Cockayne Syndrome Complex 31 0.026
788
PLM135 Palmoplantar Keratoderma, Bothnian Type 29 0.026
789
MYC015 Mycobacterium Fortuitum 27 0.026
790
MLK004 Malakoplakia 27 0.026
791
CCT001 Cicatricial Ectropion 24 0.026
792
c EPD043 Epidermolysis Bullosa Dystrophica, Ad 21 0.026
793
PSD078 Pseudofolliculitis Barbae 20 0.026
794
ERS002 Erosive Pustular Dermatosis of the Scalp 20 0.026
795
c KRT056 Keratosis Palmoplantaris Striata I, Ad 20 0.026
796
EPD052 Epidermolysis Bullosa Simplex Superficialis 20 0.026
797
c DRM040 Dermatitis Herpetiformis, Familial 18 0.026
798
c ATP020 Atopic Dermatitis 7 16 0.026
799
LNR009 Linear Atrophoderma of Moulin 14 0.026
800
P PRS040 Prostate Cancer 89 0.025
801
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.025
802
ULC004 Ulcerative Colitis 75 0.025
803
PRT036 Peritonitis 62 0.025
804
WGN006 Wegener Granulomatosis 62 0.025
805
WLL001 Williams-Beuren Syndrome 61 0.025
806
P PNC044 Pancreatitis 60 0.025
807
P ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 60 0.025
808
P PNL012 Penile Cancer 60 0.025
809
SPT004 Septic Arthritis 59 0.025
810
P MSC007 Muscle Hypertrophy 59 0.025
811
ETH011 Ethylmalonic Encephalopathy 59 0.025
812
P NTR004 Neutropenia 59 0.025
813
c SRC025 Sarcoidosis 1 58 0.025
814
P MCR010 Microcephaly 58 0.025
815
ALP001 Alopecia Universalis 57 0.025
816
P CND004 Candidiasis 57 0.025
817
P PLY017 Polyarteritis Nodosa 55 0.025
818
P MNC007 Monocytic Leukemia 55 0.025
819
P LRY019 Laryngitis 55 0.025
820
CPR001 Coproporphyria 55 0.025
821
MVM001 Movement Disease 54 0.025
822
SLP005 Sleep Disorder 53 0.025
823
c INS002 in Situ Carcinoma 52 0.025
824
P MSC033 Muscle Disorders 52 0.025
825
PRP032 Porphyria Variegata 52 0.025
826
P ERY008 Erythromelalgia 52 0.025
827
LRN003 Learning Disability 51 0.025
828
CHL069 Cholesteatoma 51 0.025
829
FML037 Female Breast Cancer 51 0.025
830
GYN001 Gynecomastia 49 0.025
831
ANT024 Anthrax Disease 48 0.025
832
P GRN010 Granular Cell Tumor 47 0.025
833
GLC008 Glucose Metabolism Disease 47 0.025
834
RPR002 Reproductive System Disease 46 0.025
835
SPH001 Sapho Syndrome 44 0.025
836
FCT008 Factitious Disorder 43 0.025
837
PRX075 Proximal Myopathy and Ophthalmoplegia 43 0.025
838
PLM029 Palmoplantar Keratosis 42 0.025
839
HYP022 Hypohidrosis 42 0.025
840
FBR019 Fibromatosis 42 0.025
841
SYR002 Syringocystadenoma Papilliferum 42 0.025
842
BND014 Bone Development Disease 42 0.025
843
CMM003 Common Wart 42 0.025
844
EGG001 Egg Allergy 42 0.025
845
PNC085 Penicillin Allergy 41 0.025
846
ACT167 Acute Generalized Exanthematous Pustulosis 40 0.025
847
NRC019 Neurocutaneous Melanosis, Somatic 39 0.025
848
FXF002 Fox-Fordyce Disease 39 0.025
849
HMN016 Hemangioendothelioma 38 0.025
850
ATM012 Autoimmune Disease of Blood 37 0.025
851
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.025
852
TNG001 Tungiasis 36 0.025
853
DRC001 Dracunculiasis 36 0.025
854
ADP001 Adiposis Dolorosa 36 0.025
855
ACR002 Acrocapitofemoral Dysplasia 36 0.025
856
HRP002 Herpes Gestationis 36 0.025
857
ECT004 Ecthyma 35 0.025
858
P PST059 Pustular Psoriasis 35 0.025
859
PLM137 Palmoplantar Keratoderma and Woolly Hair 33 0.025
860
c MLN032 Melanoma, Cutaneous Malignant, 2 33 0.025
861
BRD005 Borderline Leprosy 32 0.025
862
PRL042 Proliferating Trichilemmal Cyst 31 0.025
863
DRM003 Dermatosis Papulosa Nigra 31 0.025
864
PRK010 Porokeratosis of Mibelli 31 0.025
865
c ALB010 Albinism, Oculocutaneous, Type Ib 31 0.025
866
LBM003 Lobomycosis 30 0.025
867
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 29 0.025
868
EPD034 Epidermolysis Bullosa, Pretibial 29 0.025
869
c EHL041 Ehlers-Danlos Syndrome, Type Vii 29 0.025
870
ELS002 Elastosis Perforans Serpiginosa 28 0.025
871
c LCL022 Localized Lipodystrophy 28 0.025
872
KRT044 Keratosis Pilaris 27 0.025
873
c CTS038 Cutis Laxa, Autosomal Recessive, Type Iia 25 0.025
874
GRW032 Growth Factors, Combined Defect of 23 0.025
875
EPD057 Epidermylysis Bullosa Simplex-Mcr 20 0.025
876
c EHL065 Ehlers-Danlos Syndrome, Type V 18 0.025
877
QNQ001 Quinquaud's Decalvans Folliculitis 17 0.025
878
AND005 Androgen Insensitivity Syndrome, Mild 16 0.025
879
c PMP006 Pemphigus Vulgaris, Familial 16 0.025
880
c RTH004 Rothmund-Thomson Syndrome Type 1 13 0.025
881
c ATS003 Autosomal Recessive Type Iv Ehlers-Danlos Syndrome 9 0.025
882
P LNG032 Lung Cancer 94 0.024
883
HPT023 Hepatocellular Carcinoma 91 0.024
884
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.024
885
INS024 Insulin-Like Growth Factor I 74 0.024
886
P NRF019 Neurofibromatosis, Type 2 73 0.024
887
P LVR013 Liver Disease 72 0.024
888
P WSK001 Wiskott-Aldrich Syndrome 72 0.024
889
P MTC003 Metachromatic Leukodystrophy 71 0.024
890
P PLM036 Pulmonary Fibrosis 68 0.024
891
ACR007 Acromegaly 65 0.024
892
c HPT016 Hepatitis B 64 0.024
893
EYD002 Eye Disease 63 0.024
894
LNG099 Lung Disease 62 0.024
895
DNG002 Dengue Hemorrhagic Fever 62 0.024
896
PRM097 Primary Immunodeficiency Disease 61 0.024
897
P ASP006 Aspergillosis 60 0.024
898
P TMP003 Temporal Arteritis 60 0.024
899
P SHR029 Short Syndrome 60 0.024
900
P UVT001 Uveitis 59 0.024
901
MSS002 Mass Syndrome 59 0.024
902
P ANT006 Antiphospholipid Syndrome 58 0.024
903
P LKD001 Leukodystrophy 58 0.024
904
PRT093 Proteus Syndrome, Somatic 55 0.024
905
CCC001 Coccidioidomycosis 55 0.024
906
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.024
907
P LMY004 Leiomyosarcoma 53 0.024
908
URN009 Urinary System Disease 53 0.024
909
P INT063 Intellectual Disability 53 0.024
910
P ANG015 Angioedema 53 0.024
911
P TRT010 Teratoma 52 0.024
912
OCL020 Ocular Cicatricial Pemphigoid 52 0.024
913
PRT058 Pure Autonomic Failure 51 0.024
914
ERD001 Erdheim-Chester Disease 51 0.024
915
BRT002 Birt-Hogg-Dube Syndrome 51 0.024
916
NNT012 Neonatal Jaundice 51 0.024
917
c INF067 Inflammatory Bowel Disease 10 51 0.024
918
c XRD018 Xeroderma Pigmentosum, Group a 51 0.024
919
CHN055 Chanarin-Dorfman Syndrome 49 0.024
920
P PCH015 Pachyonychia Congenita 1 49 0.024
921
RTN023 Retinitis 49 0.024
922
FML039 Female Reproductive System Disease 48 0.024
923
MCR088 Microscopic Polyangiitis 48 0.024
924
HYP074 Hypersensitivity Vasculitis 47 0.024
925
SXL003 Sexual Disorder 47 0.024
926
OCC006 Occipital Horn Syndrome 46 0.024
927
LYM051 Lymphomatoid Granulomatosis 46 0.024
928
VLV044 Vulvar Intraepithelial Neoplasia 46 0.024
929
SCR002 Scurvy 45 0.024
930
P INF049 Infantile Myofibromatosis 45 0.024
931
DYS022 Dyschromatosis Symmetrica Hereditaria 45 0.024
932
P CNN004 Connective Tissue Cancer 45 0.024
933
HRT031 Hartnup Disorder 44 0.024
934
CHR008 Choroiditis 43 0.024
935
SPN032 Spindle Cell Carcinoma 43 0.024
936
c CLL012 Cell Type Benign Neoplasm 41 0.024
937
HYP458 Hyper Ige Syndrome 41 0.024
938
WRD025 Waardenburg Syndrome, Type 2e, with or Without Neurologic Involvement 41 0.024
939
LNR006 Linear Iga Disease 41 0.024
940
BDY001 Body Dysmorphic Disorder 41 0.024
941
EPD041 Epidermolysis Bullosa Simplex, Weber-Cockayne Type 41 0.024
942
TTR011 Tetraploidy 41 0.024
943
c JVN003 Juvenile Xanthogranuloma 40 0.024
944
MLN013 Melanoma Metastasis 40 0.024
945
TXC011 Toxocariasis 37 0.024
946
RTC008 Reticulate Acropigmentation of Kitamura 34 0.024
947
LNT002 Lentigo Maligna Melanoma 34 0.024
948
PMP002 Pemphigoid Gestationis 34 0.024
949
ORL022 Oral Erosive Lichen 33 0.024
950
OLM001 Olmsted Syndrome 33 0.024
951
DRM008 Dermatographia 33 0.024
952
HYW001 Hay-Wells Syndrome 33 0.024
953
c CTS008 Cutis Laxa, Autosomal Dominant 32 0.024
954
SCL025 Scleromyxedema 30 0.024
955
c CTS023 Cutis Laxa, Autosomal Recessive, Type Iib 28 0.024
956
SCH038 Schopf-Schulz-Passarge Syndrome 27 0.024
957
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 26 0.024
958
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 26 0.024
959
ODN009 Odontoonychodermal Dysplasia 25 0.024
960
SPN180 Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like 25 0.024
961
c APL023 Aplasia Cutis Congenita, Nonsyndromic 25 0.024
962
BRN121 Branchiootorenal/branchiootic Syndrome 25 0.024
963
BCL011 Bacillary Angiomatosis 24 0.024
964
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 24 0.024
965
P PRM145 Primary Anetoderma 20 0.024
966
DYS133 Dyschromatosis Universalis 20 0.024
967
P HYD015 Hydroa Vacciniforme 20 0.024
968
ARG004 Argyria 19 0.024
969
BLL015 Bullous Lichen Planus 19 0.024
970
ATM053 Autoimmune Disease 2 19 0.024
971
RCS008 Recessive Dystrophic Epidermolysis Bullosa-Generalized Other 18 0.024
972
c FCL046 Focal Facial Dermal Dysplasia 4 17 0.024
973
c DMN009 Dominant Ichthyosis Vulgaris 15 0.024
974
CTN031 Cutaneous Pseudolymphoma 15 0.024
975
PRK076 Porokeratosis 2, Palmar, Plantar, and Disseminated Type 13 0.024
976
c LPR019 Lipe-Related Familial Partial Lipodystrophy 8 0.024
977
MLR004 Malaria 79 0.023
978
CRH001 Crohn's Disease 76 0.023
979
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.023
980
KRT004 Keratitis 70 0.023
981
P CRD011 Cardiomyopathy 67 0.023
982
c PNC108 Pancreatitis, Hereditary 67 0.023
983
c CHR089 Chronic Kidney Failure 66 0.023
984
P MNN013 Meningitis 65 0.023
985
P HYP086 Hypothyroidism 65 0.023
986
AND015 Androgen Insensitivity 63 0.023
987
P PRD006 Prader-Willi Syndrome 63 0.023
988
P THN009 Thanatophoric Dysplasia, Type I 62 0.023
989
APH001 Aphthous Stomatitis 62 0.023
990
P ESP024 Esophagitis 62 0.023
991
c VRL010 Viral Hepatitis 61 0.023
992
OST017 Osteomyelitis 59 0.023
993
PHR003 Pharyngitis 58 0.023
994
LPM004 Lipoma 58 0.023
995
P AGM005 Agammaglobulinemia, X-Linked 1 57 0.023
996
EMB004 Embryonal Carcinoma 56 0.023
997
SFT003 Soft Tissue Sarcoma 56 0.023
998
ALK013 Alkaptonuria 55 0.023
999
HMF006 Hemifacial Microsomia 54 0.023
1000
AGN012 Agnathia-Otocephaly Complex 54 0.023
1001
P LPC002 Lip Cancer 53 0.023
1002
OSS012 Osseous Heteroplasia, Progressive 53 0.023
1003
PTT049 Pituitary Adenoma, Acth-Secreting 53 0.023
1004
P LPD010 Lipodystrophy 52 0.023
1005
P URF003 Urofacial Syndrome 1 52 0.023
1006
ADN009 Adenosquamous Carcinoma 51 0.023
1007
CRT049 Critical Limb Ischemia 51 0.023
1008
HPT074 Hepatic Adenoma, Somatic 51 0.023
1009
P DRR001 Diarrhea 51 0.023
1010
P SJG002 Sjogren-Larsson Syndrome 51 0.023
1011
PLM014 Pleomorphic Adenoma 50 0.023
1012
STM006 Stomach Disease 50 0.023
1013
PRN014 Paronychia 50 0.023
1014
PRD019 Periodic Fever, Familial 50 0.023
1015
MYL020 Myelomeningocele 50 0.023
1016
INF034 Infective Endocarditis 50 0.023
1017
STR008 Strongyloidiasis 50 0.023
1018
RHM001 Rheumatic Fever 50 0.023
1019
SPR099 Supravalvar Aortic Stenosis 49 0.023
1020
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 47 0.023
1021
c XRD019 Xeroderma Pigmentosum, Group C 47 0.023
1022
PPL046 Popliteal Pterygium Syndrome 1 47 0.023
1023
MCP006 Mucoepidermoid Carcinoma 47 0.023
1024
ATN002 Autonomic Nervous System Disease 47 0.023
1025
P TMR011 Tumoral Calcinosis, Hyperphosphatemic, Familial 46 0.023
1026
CWP001 Cowpox 46 0.023
1027
CTS002 Cat-Scratch Disease 45 0.023
1028
BNC003 Bone Cancer 45 0.023
1029
SND002 Sneddon Syndrome 44 0.023
1030
URM005 Uremic Pruritus 42 0.023
1031
MLR002 Miliary Tuberculosis 42 0.023
1032
c ATS013 Autosomal Recessive Congenital Ichthyosis 42 0.023
1033
GST078 Gastrointestinal Allergy 41 0.023
1034
BSL006 Basaloid Squamous Cell Carcinoma 41 0.023
1035
P CYS017 Cystic Teratoma 41 0.023
1036
c EHL018 Ehlers-Danlos Syndrome Type Ii 40 0.023
1037
MYC017 Mycobacterium Kansasii 40 0.023
1038
EXN001 Exanthema Subitum 40 0.023
1039
ATY008 Atypical Lipomatous Tumor 40 0.023
1040
JWC001 Jaw Cancer 39 0.023
1041
EPT011 Epithelioid Leiomyosarcoma 39 0.023
1042
NSY001 N Syndrome 39 0.023
1043
TTZ003 Tietz Albinism-Deafness Syndrome 38 0.023
1044
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 38 0.023
1045
P AXN001 Axonal Neuropathy 38 0.023
1046
EPS026 Epispadias 37 0.023
1047
ANT039 Antisynthetase Syndrome 37 0.023
1048
DRM009 Dermatomycosis 36 0.023
1049
LCH004 Lichen Disease 36 0.023
1050
ECT061 Ectodermal Dysplasia 10a, Hypohidrotic/hair/nail Type, Autosomal Dominant 36 0.023
1051
ERY046 Erythroderma, Congenital, with Palmoplantar Keratoderma, Hypotrichosis, and Hyper Ige 35 0.023
1052
VSC008 Vascular Hemostatic Disease 33 0.023
1053
KKC001 Kikuchi Disease 33 0.023
1054
c HYP373 Hyper-Ige Recurrent Infection Syndrome, Autosomal Recessive 33 0.023
1055
CHL035 Cholinergic Urticaria 32 0.023
1056
c ALB019 Albinism, Oculocutaneous, Type Iv 32 0.023
1057
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 32 0.023