Search results for "skin"

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

5353 hits were found for 'skin'

# Family MCID Name MIFTS Score
1
c PLN018 Peeling Skin Syndrome 2 36 3.994
2
SKN016 Skin Disease 69 3.599
3
c SKN012 Skin Carcinoma in Situ 43 3.400
4
c LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 41 3.265
5
P PLN008 Peeling Skin Syndrome 45 3.185
6
P ECT007 Ectodermal Dysplasia/skin Fragility Syndrome 42 3.144
7
c PLN017 Peeling Skin Syndrome 1 32 2.985
8
c PLN021 Peeling Skin Syndrome 3 30 2.973
9
STF002 Stiff Skin Syndrome 51 2.872
10
WRN004 Wrinkly Skin Syndrome 34 2.844
11
SKN023 Skin Tag 48 2.793
12
P SKN013 Skin Benign Neoplasm 38 2.686
13
SKN024 Skin Fragility-Woolly Hair Syndrome 20 2.487
14
SKN019 Skin Melanoma 61 2.470
15
SKN002 Skin Lipoma 23 2.467
16
SKN020 Skin Papilloma 33 2.359
17
SKN018 Skin Hemangioma 40 2.329
18
RTT001 Ritter's Disease 35 2.322
19
GRN032 Granulomatous Slack Skin Disease 19 2.320
20
PRN056 Parana Hard-Skin Syndrome 14 2.306
21
P SKN063 Skin Creases, Congenital Symmetric Circumferential, 1 19 2.299
22
SKN022 Skin Squamous Cell Carcinoma 41 2.233
23
SKN005 Skin Atrophy 42 2.182
24
BRB006 Barber-Say Syndrome 34 2.115
25
P RST011 Restrictive Dermopathy, Lethal 38 2.108
26
HYP346 Hypotrichosis and Recurrent Skin Vesicles 18 2.102
27
BLL007 Bullous Skin Disease 39 1.921
28
CHR100 Chronic Ulcer of Skin 32 1.914
29
P GNR027 Generalized Peeling Skin Syndrome 21 1.901
30
VSC012 Vesiculobullous Skin Disease 38 1.901
31
SKN001 Skin Angiosarcoma 13 1.889
32
NDL009 Nodular Basal Cell Carcinoma 29 1.887
33
PLN020 Peeling Skin with Leukonychia, Acral Punctate Keratoses, Cheilitis, and Knuckle Pads 16 1.880
34
PLM082 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal 17 1.880
35
SKN061 Skin Fragility-Woolly Hair-Palmoplantar Keratoderma Syndrome 10 1.875
36
MLG007 Malignant Skin Fibrous Histiocytoma 31 1.873
37
SRC008 Sarcomatoid Squamous Cell Skin Carcinoma 28 1.870
38
SKN011 Skin Pilomatrix Carcinoma 21 1.870
39
SKN008 Skin Glomus Tumor 11 1.870
40
EPD010 Epidermal Appendage Tumor 15 1.864
41
MTT001 Metatypical Basal Cell Carcinoma 14 1.864
42
TNG009 Tongue Squamous Cell Carcinoma 73 1.727
43
VSC009 Vascular Skin Disease 21 1.714
44
UVN001 Uv-Induced Skin Damage 18 1.662
45
ANG016 Angiokeratoma 43 1.650
46
JSS001 Jessner's Lymphocytic Infiltration of the Skin 13 1.650
47
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 39 1.644
48
SKN021 Skin Sarcoma 35 1.642
49
P LNR015 Linear Skin Defects with Multiple Congenital Anomalies 26 1.640
50
CLF045 Cleft, Median, of Upper Lip with Polyps of Facial Skin and Nasal Mucosa 19 1.640
51
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 20 1.636
52
c LNR014 Linear Skin Defects with Multiple Congenital Anomalies 3 16 1.636
53
CTN004 Cutaneous Fibrous Histiocytoma 41 1.636
54
SKN027 Skin Conditions 44 1.635
55
c INF144 Inflammatory Skin and Bowel Disease, Neonatal, 1 18 1.633
56
c INF146 Inflammatory Skin and Bowel Disease, Neonatal, 2 15 1.633
57
SQM001 Squamous Cell Papilloma of Skin 13 1.633
58
SKN010 Skin Epithelioid Hemangioma 14 1.631
59
P SKN009 Skin Granular Cell Tumor 15 1.628
60
VRR003 Verruciform Xanthoma of Skin 18 1.628
61
SDD003 Saddan 30 1.626
62
DRM002 Dermoid Cyst of Skin 13 1.626
63
CLR010 Clear Cell Squamous Cell Skin Carcinoma 10 1.626
64
SKN017 Skin Glomangioma 9 1.623
65
c MLG050 Malignant Granular Cell Skin Tumor 12 1.623
66
CTN002 Cutaneous Mucoepidermoid Carcinoma 23 1.623
67
ECC006 Eccrine Mixed Tumor of Skin 7 1.623
68
BSL002 Basaloid Squamous Cell Skin Carcinoma 8 1.623
69
ACN008 Acantholytic Squamous Cell Skin Carcinoma 6 1.623
70
P EHL001 Ehlers-Danlos Syndrome 61 1.399
71
MVD001 Moved to 60 1.373
72
HYP542 Hypersensitivity Syndrome, Carbamazepine-Induced 51 1.364
73
KPS004 Kaposi Sarcoma 69 1.362
74
ATM016 Autoimmune Disease of Skin and Connective Tissue 30 1.362
75
KWS001 Kwashiorkor 45 1.356
76
SKN006 Skin Sarcoidosis 34 1.354
77
NRT002 Neurotic Excoriation 30 1.352
78
P NNT037 Neonatal Inflammatory Skin and Bowel Disease 21 1.346
79
EXF006 Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-Like 21 1.343
80
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 34 1.343
81
CTN013 Cutaneous Anthrax 35 1.343
82
P CPL006 Capillary Hemangioma 53 1.343
83
MLT104 Multiple Benign Circumferential Skin Creases on Limbs 20 1.343
84
DYS044 Dysmorphism Cleft Palate Loose Skin 10 1.341
85
MCR095 Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 28 1.338
86
EYB005 Eyebrows, Duplication of, with Stretchable Skin and Syndactyly 13 1.338
87
c ALB017 Albinism, Oculocutaneous, Type Vi 28 1.336
88
c SKN062 Skin Creases, Congenital Symmetric Circumferential, 2 10 1.336
89
RDS002 Red Skin Pigment Anomaly of New Guinea 6 1.336
90
LYM008 Lymphangiosarcoma 48 1.333
91
c GNR024 Generalized Peeling Skin Syndrome Type C 12 1.333
92
CND003 Candidal Paronychia 11 1.329
93
MNT259 Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies 14 1.329
94
CTN009 Cutaneous Adenocystic Carcinoma 30 1.329
95
PRN012 Perianal Skin Paget's Disease 7 1.329
96
CTN010 Cutaneous Ganglioneuroma 25 1.329
97
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 6 1.329
98
SKN004 Skin Amelanotic Melanoma 6 1.329
99
SKN007 Skin Meningioma 9 1.329
100
PLN004 Plantar Verrucous Skin Carcinoma 5 1.329
101
ECC008 Eccrine Sweat Gland Neoplasm 24 1.326
102
WND001 Wound Botulism 31 1.326
103
CLR015 Clear Cell Basal Cell Carcinoma 23 1.326
104
CRS012 Carasil Syndrome 30 1.322
105
ADM002 Adamantinoid Basal Cell Epithelioma 10 1.322
106
CTN001 Cutaneous Solitary Mastocytoma 26 1.322
107
SGN001 Signet Ring Basal Cell Carcinoma 6 1.322
108
SRC003 Sarcomatoid Basal Cell Carcinoma 10 1.322
109
DRM006 Dermatitis 58 1.267
110
c BSL007 Basal Cell Carcinoma 66 1.127
111
c DWL002 Dowling-Degos Disease 1 33 1.039
112
ADR038 Adermatoglyphia 39 1.036
113
P CTS001 Cutis Laxa 57 1.035
114
P DRM010 Dermatomyositis 59 1.032
115
PMS001 Poems Syndrome 56 1.013
116
CNG008 Congenital Ichthyosiform Erythroderma 52 0.994
117
P APL006 Aplasia Cutis Congenita 48 0.991
118
HDR004 Hidradenoma 32 0.989
119
P SBR004 Seborrheic Dermatitis 41 0.987
120
P ANG013 Angioma Serpiginosum 29 0.982
121
BLM001 Bloom Syndrome 63 0.978
122
GNT020 Giant Congenital Nevus 23 0.978
123
MCH008 Michelin Tire Baby Syndrome 13 0.978
124
MLT122 Multiple Self-Healing Squamous Epithelioma, Susceptiblity to 27 0.976
125
ACR014 Acral Lentiginous Melanoma 44 0.974
126
P SPR013 Spiradenoma 37 0.974
127
AML001 Amelanotic Melanoma 40 0.974
128
BRK001 Brooke-Spiegler Syndrome 47 0.972
129
KRT013 Keratolytic Winter Erythema 25 0.972
130
CHN002 Chancroid 37 0.972
131
APH001 Aphthous Stomatitis 62 0.968
132
CTN012 Cutaneous Leiomyosarcoma 38 0.968
133
ESN002 Eosinophilia-Myalgia Syndrome 45 0.965
134
P CRN038 Carney Complex Variant 53 0.963
135
CTN027 Cutaneous Mastocytoma 23 0.963
136
MCC010 Mccune-Albright Syndrome, Somatic, Mosaic 58 0.960
137
NXS001 Naxos Disease 46 0.960
138
PSD059 Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency 23 0.960
139
DRM042 Dermatoosteolysis, Kirghizian Type 16 0.960
140
c PLL014 Pellagra-Like Syndrome 18 0.960
141
ADN015 Adenoid Basal Cell Carcinoma 36 0.960
142
KSK002 Kosaki Overgrowth Syndrome 17 0.958
143
MCR036 Macroepiphyseal Dysplasia with Osteoporosis, Wrinkled Skin, and Aged Appearance 9 0.958
144
PSD101 Pseudoxanthoma Elasticum-Like Skin Manifestations with Retinitis Pigmentosa 7 0.958
145
SPR107 Sparse Hair-Short Stature-Skin Anomalies Syndrome 8 0.958
146
c GRS013 Griscelli Syndrome, Type 1 34 0.955
147
P FNC043 Fanconi Anemia, Complementation Group E 45 0.955
148
FLY003 Flynn-Aird Syndrome 17 0.955
149
EBD002 Ebd, Bart Type 13 0.955
150
c MLG049 Malignant Syringoma 19 0.955
151
P WVR001 Weaver Syndrome 54 0.952
152
P MLN043 Melanoma, Cutaneous Malignant 8 36 0.952
153
NGL001 Naegeli-Franceschetti-Jadassohn Syndrome 30 0.952
154
c MCL040 Macular Degeneration, Age-Related, 3 31 0.952
155
MCR274 Microcephalic Primordial Dwarfism, Montreal Type 17 0.952
156
CTN006 Cutaneous Paget's Disease 23 0.952
157
ECC004 Eccrine Porocarcinoma 33 0.952
158
BRS103 Bier Spots 13 0.952
159
HLL006 Halal Setton Wang Syndrome 14 0.952
160
SNL003 Senile Angioma 32 0.952
161
HRD105 Hereditary Sensorimotor Neuropathy with Hyperelastic Skin 4 0.952
162
PGM025 Pigmentation Defects-Palmoplantar Keratoderma-Skin Carcinoma Syndrome 5 0.952
163
ICH027 Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 5 0.952
164
MNT019 Mental Retardation Hypotonia Skin Hyperpigmentation 3 0.952
165
MSM009 Mesomelic Dysplasia Skin Dimples 3 0.952
166
SHR013 Short Stature Abnormal Skin Pigmentation Mental Retardation 3 0.952
167
c DSP002 Dsp-Related Ectodermal Dysplasia/skin Fragility Syndrome 6 0.952
168
c PKP001 Pkp1-Related Ectodermal Dysplasia/skin Fragility Syndrome 6 0.952
169
CMB022 Combined Cellular and Humoral Immune Defects with Granulomas 30 0.948
170
ANG065 Angioma, Tufted 22 0.948
171
HDR001 Hidrocystoma 25 0.948
172
ANL016 Anal Margin Carcinoma 20 0.948
173
FCL068 Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome 18 0.948
174
END012 Endometriosis in Scar of Skin 5 0.948
175
SQR001 Sequeiros Sack Syndrome 6 0.948
176
CYS004 Cystic Basal Cell Carcinoma 26 0.948
177
INT287 Intellectual Disability-Hypotonia-Skin Hyperpigmentation Syndrome 11 0.948
178
PGM002 Pigmented Basal Cell Carcinoma 27 0.948
179
SKN026 Skin Cancer, Non Melanoma, Childhood 8 0.948
180
WDH003 Woodhouse-Sakati Syndrome 32 0.944
181
TNL002 Toenail Dystrophy, Isolated 19 0.944
182
CRN070 Corneodermatoosseous Syndrome 18 0.944
183
DNT019 Daentl Towsend Siegel Syndrome 15 0.944
184
c MLG048 Malignant Acrospiroma 14 0.944
185
ECC001 Eccrine Papillary Adenocarcinoma 15 0.944
186
P APL009 Aplasia Cutis Congenita of Limbs Recessive 6 0.944
187
NVF002 Nevi Flammei 12 0.944
188
RYM001 Roy Maroteaux Kremp Syndrome 7 0.944
189
SPR033 Superficial Spreading Melanoma 17 0.944
190
INF027 Infiltrative Basal Cell Carcinoma 26 0.944
191
GLL032 Galloway-Mowat Syndrome 52 0.940
192
LMY001 Leiomyoma Cutis 24 0.940
193
ALG003 Al Gazali Aziz Salem Syndrome 12 0.940
194
ECC002 Eccrine Acrospiroma 23 0.940
195
PLM113 Palmoplantar Keratoderma-Sclerodactyly Syndrome 8 0.940
196
SBC009 Sebaceous Adenoma 35 0.940
197
HRY007 Hairy Palms and Soles 8 0.940
198
TNG005 Tang Hsi Ryu Syndrome 7 0.940
199
ECC003 Eccrine Papillary Adenoma 11 0.940
200
GRB001 Grubben De Cock Borghgraef Syndrome 7 0.940
201
JDG001 Judge Misch Wright Syndrome 6 0.940
202
JNS005 Jones Hersh Yusk Syndrome 8 0.940
203
INF028 Infundibulocystic Basal Cell Carcinoma 28 0.940
204
THM006 Thumb Deformity, Alopecia, Pigmentation Anomaly 8 0.940
205
ANL007 Anal Margin Squamous Cell Carcinoma 13 0.940
206
ANL013 Anal Margin Basal Cell Carcinoma 12 0.940
207
CPL002 Capillary Lymphangioma 17 0.940
208
BNG008 Benign Dermal Neurilemmoma 9 0.940
209
MLT066 Multiple Cutaneous and Uterine Leiomyomas 16 0.940
210
MST010 Mastocytosis Cutaneous with Short Stature Conductive Hearing Loss and Microtia 6 0.940
211
c WVR003 Weaver Syndrome 1 19 0.940
212
DRM001 Dermal Unilateral Segmental Cavernous Angioma 6 0.940
213
CTN008 Cutaneous Liposarcoma 9 0.940
214
BDH001 Boudhina Yedes Khiari Syndrome 5 0.940
215
ELL003 Elliott Ludman Teebi Syndrome 4 0.940
216
ANG030 Angiomatosis, Diffuse Corticomeningeal, of Divry and Van Bogaert 4 0.940
217
MCR016 Micronodular Basal Cell Carcinoma 10 0.940
218
MGR004 Megarbane Jalkh Syndrome 4 0.940
219
MLN017 Milner Khallouf Gibson Syndrome 4 0.940
220
RVL001 Ruvalcaba Churesigaew Myhre Syndrome 4 0.940
221
c LTH013 Lethal Restrictive Dermopathy, Lmna-Related 7 0.940
222
c LTH014 Lethal Restrictive Dermopathy, Zmpste24-Related 7 0.940
223
SBC013 Sebaceous Basal Cell Carcinoma 5 0.940
224
P PSR002 Psoriasis 63 0.201
225
MLN008 Melanoma 61 0.182
226
CTN007 Cutaneous Leishmaniasis 62 0.165
227
P ATP001 Atopic Dermatitis 60 0.144
228
BRN106 Burns 52 0.117
229
P LYM118 Lymphoma 68 0.112
230
ADM013 Adamantinoma of Long Bones 57 0.108
231
KRT009 Keratosis 50 0.093
232
ACN011 Acne 63 0.090
233
EPD016 Epidermolysis Bullosa 59 0.089
234
ACT008 Actinic Keratosis 53 0.089
235
AYM001 Ayme-Gripp Syndrome 40 0.085
236
ATP002 Atopy 62 0.084
237
CNT047 Contact Dermatitis 62 0.084
238
ALL026 Allergic Hypersensitivity Disease 53 0.082
239
P LPS004 Lupus Erythematosus 63 0.081
240
MYC006 Mycosis Fungoides 66 0.080
241
URT039 Urticaria 58 0.079
242
PRM025 Primary Bacterial Infectious Disease 42 0.077
243
WRN005 Wrinkles 35 0.076
244
TBR010 Tuberculosis 70 0.075
245
PMP001 Pemphigus 49 0.074
246
CLL003 Cellulitis 49 0.072
247
P LPR003 Leprosy 70 0.070
248
P LKM002 Leukemia 70 0.070
249
BLL006 Bullous Pemphigoid 59 0.070
250
P NRP001 Neuropathy 57 0.070
251
P EXN002 Exanthem 57 0.070
252
CNN005 Connective Tissue Disease 60 0.069
253
P ART022 Arthritis 73 0.068
254
RSC001 Rosacea 54 0.068
255
END072 Endotheliitis 41 0.067
256
ALL010 Allergic Contact Dermatitis 58 0.066
257
P HRP006 Herpes Simplex 65 0.065
258
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.065
259
P PSD087 Pseudoxanthoma Elasticum 65 0.064
260
EPD001 Epidermodysplasia Verruciformis 48 0.064
261
PPL022 Papilloma 54 0.063
262
IMP004 Impetigo 41 0.062
263
P BRS047 Breast Cancer 100 0.062
264
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 54 0.062
265
P CTN015 Cutaneous T Cell Lymphoma 41 0.061
266
P SYS005 Systemic Scleroderma 60 0.059
267
MRK001 Merkel Cell Carcinoma 56 0.059
268
BRN105 Burn Scar 36 0.059
269
P DRM007 Dermatitis Herpetiformis 48 0.058
270
c LCL006 Localized Scleroderma 60 0.058
271
PGM003 Pigmentation Disease 34 0.058
272
PLM102 Palmoplantar Keratoderma, Epidermolytic 46 0.056
273
P SYN001 Syndactyly 49 0.056
274
CLV009 Clove Syndrome, Somatic 41 0.055
275
MCR013 Microphthalmia 57 0.055
276
SRC014 Sarcoma 66 0.055
277
ALP008 Alopecia 56 0.055
278
P HMN010 Hemangioma 62 0.055
279
FCL001 Facial Dermatosis 24 0.055
280
P KRT005 Keratoacanthoma 41 0.055
281
NTH001 Netherton Syndrome 52 0.055
282
ALR002 Al-Raqad Syndrome 36 0.055
283
KLD001 Keloids 50 0.055
284
P PMP005 Pemphigus Vulgaris 47 0.055
285
P THY032 Thyroiditis 57 0.054
286
P PLY019 Polyneuropathy 53 0.054
287
HDR002 Hidradenitis Suppurativa 53 0.054
288
PYD002 Pyoderma 46 0.054
289
P NRV006 Nervous System Cancer 62 0.053
290
P AST005 Asthma 80 0.052
291
PSR001 Psoriatic Arthritis 64 0.052
292
PYD001 Pyoderma Gangrenosum 48 0.052
293
P CTN003 Cutaneous Lupus Erythematosus 49 0.052
294
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 53 0.052
295
LYM006 Lymphoepithelioma-Like Carcinoma 42 0.052
296
ECT006 Ectodermal Dysplasia 46 0.052
297
c BSL024 Basal Cell Carcinoma 1 44 0.051
298
EPD006 Epidermolysis Bullosa Acquisita 46 0.051
299
DBT062 Diabetic Foot Ulcers 55 0.051
300
KND001 Kindler Syndrome 54 0.050
301
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.050
302
DRM014 Dermatofibrosarcoma Protuberans 61 0.050
303
CRC006 Carcinoid Syndrome 51 0.050
304
P RHN004 Rhinitis 59 0.050
305
HYP457 Hypertrophic Scars 45 0.050
306
c SYS001 Systemic Lupus Erythematosus 87 0.049
307
INC021 Incontinentia Pigmenti 57 0.049
308
P INF032 Infertility 61 0.049
309
C3D001 C3 Deficiency 50 0.049
310
SCB001 Scabies 45 0.049
311
IRR003 Irritant Dermatitis 45 0.049
312
c DRM035 Dermatitis, Atopic 2 29 0.049
313
c BSL025 Basal Cell Carcinoma 2 18 0.049
314
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.049
315
MLG108 Malignant Melanoma, Somatic 60 0.049
316
ACR041 Acromelic Frontonasal Dysostosis 45 0.049
317
ERY003 Erythema Multiforme 57 0.049
318
P MDL005 Medulloblastoma 76 0.048
319
P EPD003 Epidermolysis Bullosa Simplex 50 0.048
320
WLL006 Wells Syndrome 57 0.048
321
NRN004 Neuroendocrine Tumor 54 0.048
322
c PRM023 Pre-Malignant Neoplasm 42 0.048
323
LSH001 Leishmaniasis 63 0.047
324
P MST009 Mastocytosis 54 0.047
325
P PNM007 Pneumonia 67 0.047
326
P BCL006 B-Cell Lymphomas 64 0.047
327
P OBS005 Obesity 91 0.047
328
P PRP003 Porphyria Cutanea Tarda 63 0.047
329
P ALP009 Alopecia Areata 62 0.047
330
c CHR579 Chiari Malformation Type Ii 38 0.047
331
VSC011 Vasculitis 62 0.047
332
c CLL013 Cell Type Cancer 46 0.047
333
EWN003 Ewing Sarcoma 63 0.046
334
ALL003 Allergic Rhinitis 67 0.046
335
CTS003 Coats Disease 57 0.046
336
OCL009 Ocular Cancer 61 0.046
337
LGD001 Leg Dermatosis 17 0.046
338
MLL001 Molluscum Contagiosum 44 0.046
339
GRN007 Granuloma Annulare 35 0.046
340
BSC001 Buschke-Ollendorff Syndrome 59 0.045
341
P HPT021 Hepatitis 74 0.045
342
P NLD001 Nail Disease 56 0.045
343
P ESN007 Eosinophilia 61 0.045
344
PRP030 Purpura 60 0.045
345
P PRK001 Porokeratosis 45 0.045
346
DSC009 Discoid Lupus Erythematosus 40 0.045
347
P SYR003 Syringoma 37 0.045
348
NRN002 Neuronitis 40 0.045
349
P CLR023 Colorectal Cancer 96 0.044
350
DCB001 Decubitus Ulcer 44 0.044
351
P SYP003 Syphilis 51 0.044
352
P LFR001 Li-Fraumeni Syndrome 79 0.044
353
P TBR001 Tuberous Sclerosis 68 0.044
354
FCL009 Focal Dermal Hypoplasia 52 0.044
355
TST021 Testicular Germ Cell Tumor 67 0.044
356
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 47 0.044
357
ECT005 Ectropion 38 0.044
358
BRT030 Birth Defects 44 0.044
359
CLC001 Calciphylaxis 40 0.044
360
ULC005 Ulcer of Lower Limbs 21 0.044
361
GRM001 Germ Cell and Embryonal Cancer 38 0.044
362
BRS090 Breast Reconstruction 38 0.044
363
ERY021 Erythrokeratodermia Variabilis Et Progressiva 48 0.043
364
P ICH001 Ichthyosis Vulgaris 44 0.043
365
CHL071 Child Syndrome 58 0.043
366
P HYP040 Hypospadias 58 0.043
367
P ADN016 Adenocarcinoma 69 0.043
368
HDR003 Hidradenitis 46 0.043
369
P EHL033 Ehlers-Danlos Syndrome, Classic Type 55 0.042
370
P XRD010 Xeroderma Pigmentosum, Variant Type 58 0.042
371
KDS001 Kid Syndrome 53 0.042
372
DRM011 Dermatophytosis 44 0.042
373
P LCH002 Lichen Planus 61 0.042
374
PHT003 Phototoxic Dermatitis 37 0.042
375
PMP004 Pemphigus Foliaceus 42 0.042
376
P DYS007 Dyskeratosis Congenita 64 0.041
377
PCK002 Pick Disease 66 0.041
378
URB001 Urbach-Wiethe Disease 48 0.041
379
MTH009 Mouth Disease 63 0.041
380
ACN002 Acanthosis Nigricans 59 0.041
381
c PND001 Pain Disorder 53 0.041
382
MYC019 Mycobacterium Marinum 30 0.041
383
HLY001 Hailey-Hailey Disease 53 0.041
384
P PRP029 Porphyria 56 0.041
385
NSD001 Nose Disease 51 0.041
386
P OCL002 Oculocutaneous Albinism 51 0.041
387
DBT010 Diabetic Neuropathy 55 0.041
388
c RNL016 Renal Infectious Disease 22 0.041
389
P RHM011 Rheumatoid Arthritis 87 0.040
390
TNP001 Tinea Pedis 38 0.040
391
ABL002 Ablepharon-Macrostomia Syndrome 51 0.040
392
CDS001 Cadasil 50 0.040
393
LPR001 Lepromatous Leprosy 50 0.040
394
LYM052 Lymphomatoid Papulosis 45 0.040
395
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.040
396
PRT011 Protein C Deficiency 52 0.040
397
PRS047 Prostatitis 56 0.040
398
FLL008 Folliculitis 47 0.040
399
BLL012 Bullous Impetigo 28 0.040
400
CMP010 Complex Regional Pain Syndrome 59 0.039
401
P HST010 Histiocytosis 56 0.039
402
HND001 Hand Dermatosis 25 0.039
403
BRS051 Breast Disease 57 0.039
404
PNN001 Panniculitis 47 0.039
405
PTY001 Pityriasis Rosea 42 0.039
406
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.039
407
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.038
408
P EPD002 Epidermolytic Hyperkeratosis 51 0.038
409
P RTH001 Rothmund-Thomson Syndrome 56 0.038
410
ADL002 Adult Syndrome 53 0.038
411
HYP077 Hypertrichosis 52 0.038
412
VSC007 Vascular Disease 51 0.038
413
YWS001 Yaws 41 0.038
414
P VNS003 Venous Insufficiency 53 0.038
415
VND001 Vein Disease 51 0.038
416
P SML001 Small Cell Carcinoma 54 0.038
417
URT001 Urethritis 39 0.038
418
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.038
419
VRR004 Verrucous Carcinoma 54 0.038
420
VCC001 Vaccinia 46 0.038
421
ISC004 Ischemia 56 0.038
422
c EHL057 Ehlers-Danlos Syndrome, Type Iv 59 0.037
423
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.037
424
CHC001 Chickenpox 50 0.037
425
P JNC001 Junctional Epidermolysis Bullosa 52 0.037
426
LYM024 Lymphatic System Disease 49 0.037
427
c PSR017 Psoriasis 2 29 0.037
428
PLL012 Pollen Allergy 43 0.037
429
GLB003 Globe Disease 34 0.037
430
c BSL026 Basal Cell Carcinoma 3 18 0.037
431
RDT005 Radiation Induced Cancer 26 0.037
432
PTY003 Pityriasis Rubra Pilaris 46 0.037
433
HRP004 Herpes Zoster 56 0.037
434
P EPD009 Epidermolysis Bullosa Dystrophica 55 0.037
435
ICH031 Ichthyosis with Confetti 27 0.037
436
P ANP001 Anaplastic Large Cell Lymphoma 58 0.037
437
SCL022 Scleredema 27 0.037
438
c ADL017 Adult T-Cell Leukemia 59 0.037
439
ERY017 Erythema Elevatum Diutinum 39 0.037
440
ALL006 Allergic Asthma 59 0.037
441
FDL002 Food Allergy 56 0.037
442
NCR002 Necrobiosis Lipoidica 33 0.037
443
URT008 Urticaria Pigmentosa 37 0.037
444
FSC004 Fasciitis 47 0.037
445
c SBC035 Subacute Cutaneous Lupus Erythematosus 47 0.037
446
IMM127 Immune System Cancer 41 0.037
447
SML033 Small Cell Cancer of the Lung, Somatic 53 0.036
448
PBL001 Piebaldism 56 0.036
449
PRL019 Prolidase Deficiency 39 0.036
450
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 33 0.036
451
SZR001 Sezary's Disease 51 0.036
452
LYM019 Lymphosarcoma 52 0.036
453
MLR001 Miliaria Rubra 26 0.036
454
c SCL052 Scleroderma, Familial Progressive 27 0.036
455
ALB002 Albinism 43 0.036
456
PRN049 Paraneoplastic Pemphigus 40 0.036
457
BSL036 Basal Cell Nevus Syndrome 65 0.035
458
DRR010 Darier Disease 60 0.035
459
c ICH041 Ichthyosis, Autosomal Recessive 4b 35 0.035
460
MLK003 Melkersson-Rosenthal Syndrome 52 0.035
461
CCT002 Cicatricial Pemphigoid 50 0.035
462
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 36 0.035
463
INC022 Inclusion-Cell Disease 46 0.035
464
c ICH040 Ichthyosis, Congenital, Autosomal Recessive 4a 24 0.035
465
NTR042 Neutrophilic Dermatosis, Acute Febrile 31 0.035
466
c ICH050 Ichthyosis, Congenital, Autosomal Recessive 5 24 0.035
467
c ICH042 Ichthyosis, Congenital, Autosomal Recessive 6 25 0.035
468
c ICH038 Ichthyosis, Congenital, Autosomal Recessive 3 24 0.035
469
c ICH044 Ichthyosis, Congenital, Autosomal Recessive 8 21 0.035
470
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 36 0.035
471
c ICH039 Ichthyosis, Congenital, Autosomal Recessive 10 20 0.035
472
PRT014 Protein S Deficiency 54 0.035
473
ACR034 Acrogeria, Gottron Type 28 0.035
474
c ICH048 Ichthyosis, Congenital, Autosomal Recessive 9 21 0.035
475
P LTR001 Lateral Sclerosis 50 0.035
476
TNC003 Tinea Corporis 38 0.035
477
c CTS019 Cutis Laxa, Ad 26 0.035
478
ANH002 Anhidrosis 42 0.035
479
c CHR417 Chronic Graft Versus Host Disease 50 0.035
480
P MYL007 Myeloma 52 0.035
481
P ACT135 Acute Graft Versus Host Disease 52 0.035
482
P PRP034 Purpura Fulminans 41 0.035
483
ACR005 Acrodermatitis 33 0.035
484
HST009 Histiocytoma 47 0.035
485
P TCL004 T-Cell Leukemia 44 0.035
486
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.034
487
c EHL055 Ehlers-Danlos Syndrome, Type Iii 49 0.034
488
LYM115 Lymphoma, Non-Hodgkin 64 0.034
489
EPD028 Epidermolysis Bullosa Simplex, Dowling-Meara Type 41 0.034
490
PRP027 Peripheral Vascular Disease 69 0.034
491
EPD062 Epidermolysis Bullosa, Junctional, Non-Herlitz Type 40 0.034
492
TRC010 Trichotillomania 39 0.034
493
P HRD018 Hair Disease 48 0.034
494
LYM017 Lyme Disease 64 0.034
495
ANG061 Angular Cheilitis 32 0.034
496
ONC002 Onchocerciasis 53 0.034
497
GRV012 Grover's Disease 39 0.034
498
HTC002 Hutchinson-Gilford Progeria 51 0.034
499
DFF003 Diffuse Scleroderma 39 0.034
500
PRP005 Parapsoriasis 40 0.034
501
CTS011 Cutis Marmorata Telangiectatica Congenita 31 0.034
502
LCH011 Lichen Planopilaris 40 0.034
503
P CLL015 Collagen Disease 49 0.034
504
P AMY004 Amyloidosis 63 0.034
505
ERY004 Erysipelas 39 0.034
506
SBC017 Sebaceous Gland Disease 35 0.034
507
MLR009 Miliaria 31 0.034
508
LPD014 Lipodermatosclerosis 36 0.034
509
PHY002 Physical Disorder 43 0.034
510
URT037 Urethral Stricture 33 0.034
511
c ADL001 Adult Lymphoma 40 0.034
512
WRN001 Werner Syndrome 69 0.033
513
BLS001 Blau Syndrome 59 0.033
514
c ALB021 Albinism, Oculocutaneous, Type Ii 41 0.033
515
P PCH001 Pachyonychia Congenita 54 0.033
516
P MYP004 Myopathy 67 0.033
517
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 34 0.033
518
ACR003 Acrodermatitis Enteropathica 49 0.033
519
EYD002 Eye Disease 62 0.033
520
EPD022 Epidermolysis Bullosa Pruriginosa 39 0.033
521
c EHL054 Ehlers-Danlos Syndrome, Type Vi 42 0.033
522
CHR031 Chromoblastomycosis 43 0.033
523
NPH018 Nephrogenic Systemic Fibrosis 51 0.033
524
HRZ001 Huriez Syndrome 33 0.033
525
VSC006 Vascular Cancer 51 0.033
526
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.033
527
LCH009 Lichen Sclerosus 43 0.033
528
c BSL011 Basal Cell Carcinoma, Multiple 21 0.033
529
ART006 Arthus Reaction 40 0.033
530
P END033 Endocarditis 52 0.033
531
ERY010 Erythrasma 20 0.033
532
HYP213 Hypomelanotic Disorder 20 0.033
533
ORL011 Oral Cancer 53 0.033
534
ANG020 Angiosarcoma 53 0.033
535
c SCN006 Secondary Syphilis 41 0.033
536
c BSL028 Basal Cell Carcinoma 5 18 0.033
537
c CHR431 Chronic Venous Insufficiency 43 0.033
538
c BCT003 Bacterial Exanthem 13 0.033
539
ADR007 Adrenoleukodystrophy 74 0.032
540
FBR012 Fabry Disease 68 0.032
541
BRN024 Bronchitis 67 0.032
542
ETH011 Ethylmalonic Encephalopathy 57 0.032
543
CST001 Costello Syndrome 68 0.032
544
MND007 Mandibuloacral Dysplasia 51 0.032
545
P MRT001 Muir-Torre Syndrome 59 0.032
546
c EHL032 Ehlers-Danlos Syndrome, Type Viib 48 0.032
547
P NRV007 Nervous System Disease 71 0.032
548
CLR065 Colorectal Adenomatous Polyposis, Autosomal Recessive, with Pilomatricomas 46 0.032
549
c HPT001 Hepatitis C 68 0.032
550
STT007 Steatocystoma Multiplex 45 0.032
551
P ART023 Arthropathy 63 0.032
552
P MSC005 Muscular Dystrophy 64 0.032
553
P CCK001 Cockayne Syndrome 58 0.032
554
YLL001 Yellow Nail Syndrome 48 0.032
555
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.032
556
P SNS014 Sinusitis 66 0.032
557
ALN001 Aland Island Eye Disease 45 0.032
558
c CTS031 Cutis Laxa, Autosomal Dominant 2 23 0.032
559
LYM021 Lymphadenitis 58 0.032
560
SML019 Smallpox 49 0.032
561
LMT001 Limited Scleroderma 46 0.032
562
LPD004 Lipoid Nephrosis 49 0.032
563
PST062 Pustulosis Palmaris Et Plantaris 48 0.032
564
ACR097 Acrodermatitis Chronica Atrophicans 35 0.032
565
FBR003 Fibrous Histiocytoma 46 0.032
566
PYG006 Pyogenic Granuloma 47 0.032
567
c ICH045 Ichthyosis, Congenital, Autosomal Recessive 7 13 0.032
568
ORL015 Oral Squamous Cell Carcinoma 55 0.032
569
HRD113 Hereditary Acrokeratotic Poikiloderma, Weary Type 14 0.032
570
c MLT019 Multiple Myeloma 77 0.031
571
P RNL014 Renal Cell Carcinoma 80 0.031
572
MNK001 Menkes Disease 61 0.031
573
EPD053 Epidermal Nevus, Somatic 51 0.031
574
c EHL027 Ehlers-Danlos Syndrome, Type Viic 33 0.031
575
LNG024 Langerhans-Cell Histiocytosis 64 0.031
576
CYL004 Cylindromatosis, Familial 31 0.031
577
EPD056 Epidermolysis Bullosa Simplex-Mp 34 0.031
578
c PSR021 Psoriasis 14, Pustular 35 0.031
579
PRP019 Peripheral Nervous System Disease 52 0.031
580
CHR063 Chronic Mucocutaneous Candidiasis 61 0.031
581
EYL005 Eyelid Disease 41 0.031
582
P HRM001 Hermansky-Pudlak Syndrome 56 0.031
583
ICH054 Ichthyosis, X-Linked 46 0.031
584
RYN003 Reynolds Syndrome 49 0.031
585
P RBL001 Rubella 54 0.031
586
OMN001 Omenn Syndrome 61 0.031
587
PLM029 Palmoplantar Keratosis 40 0.031
588
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 35 0.031
589
RHM027 Rheumatic Disease 55 0.031
590
SPT005 Spotted Fever 56 0.031
591
EPD061 Epidermolysis Bullosa, Junctional, Herlitz Type 36 0.031
592
NRM005 Neuromuscular Disease 56 0.031
593
ACQ007 Acquired Immunodeficiency Syndrome 60 0.031
594
c TRC078 Trichohepatoenteric Syndrome 2 30 0.031
595
ECZ002 Eczema Herpeticum 46 0.031
596
P DWL001 Dowling-Degos Disease 41 0.031
597
P DRR001 Diarrhea 60 0.031
598
RFL001 Reflex Sympathetic Dystrophy 45 0.031
599
CHL056 Cheilitis 48 0.031
600
MLT016 Multicentric Reticulohistiocytosis 46 0.031
601
END030 End Stage Renal Failure 53 0.031
602
RDN001 Reading Disorder 39 0.031
603
c CTS037 Cutis Laxa, Autosomal Recessive, Type Ib 21 0.031
604
HND002 Hand, Foot and Mouth Disease 49 0.031
605
CLN019 Colonic Disease 50 0.031
606
ADN002 Adenoiditis 38 0.031
607
JNT002 Joint Disorders 55 0.031
608
ENT005 Entropion 30 0.031
609
ACT164 Actinic Prurigo 40 0.031
610
INT221 Intravascular Large B-Cell Lymphoma 37 0.031
611
CRB009 Cerebritis 36 0.031
612
CHR415 Chronic Venous Leg Ulcers 31 0.031
613
BTN003 Biotinidase Deficiency 56 0.030
614
P KDN017 Kidney Cancer 67 0.030
615
c ALB009 Albinism, Oculocutaneous, Type Ia 39 0.030
616
GST019 Gastrointestinal Stromal Tumor 73 0.030
617
P CRD013 Cardiofaciocutaneous Syndrome 65 0.030
618
P ZLL001 Zellweger Syndrome 49 0.030
619
EPD047 Epidermolysis Bullosa Simplex, Koebner Type 37 0.030
620
P EHL015 Ehlers-Danlos Syndrome Progeroid Type 39 0.030
621
P CNJ013 Conjunctivitis 65 0.030
622
c XRD015 Xeroderma Pigmentosum, Group F 45 0.030
623
MLD003 Meleda Disease 27 0.030
624
TRN023 Transient Bullous of the Newborn 25 0.030
625
P MLT048 Multiple Familial Trichoepithelioma 29 0.030
626
c MCR129 Microvascular Complications of Diabetes 1 55 0.030
627
FCL045 Focal Facial Dermal Dysplasia 3, Setleis Type 23 0.030
628
P LYM025 Lymphedema 60 0.030
629
CRC001 Cercarial Dermatitis 40 0.030
630
c SYS004 Systemic Mastocytosis 60 0.030
631
PLM137 Palmoplantar Keratoderma and Woolly Hair 34 0.030
632
MST017 Mast Cell Disease 52 0.030
633
CRY004 Cryoglobulinemia 47 0.030
634
PLC008 Placenta Disease 33 0.030
635
P INT063 Intellectual Disability 46 0.030
636
PLM001 Pulmonary Tuberculosis 69 0.030
637
P SPS003 Spastic Diplegia 49 0.030
638
P PLL002 Pellagra 43 0.030
639
GRD005 Geroderma Osteodysplasticum 27 0.030
640
ATM052 Autoimmune Disease 1 26 0.030
641
PLS011 Plasmacytoma 57 0.030
642
c AST037 Asthma 1 35 0.030
643
ADN018 Adenoma 59 0.030
644
SBC012 Subcorneal Pustular Dermatosis 39 0.030
645
P GRN010 Granular Cell Tumor 46 0.030
646
BCT015 Bacteremia 50 0.030
647
P ICH023 Ichthyosis, Acquired 20 0.030
648
P HYP087 Hypotrichosis 44 0.030
649
MLK004 Malakoplakia 28 0.030
650
PST053 Postherpetic Neuralgia 41 0.030
651
MYC013 Mycobacterium Abscessus 41 0.030
652
SLR005 Solar Urticaria 20 0.030
653
LYM023 Lymphatic System Cancer 35 0.030
654
WTH001 Withdrawal Disorder 36 0.030
655
SCR033 Scar Contracture 24 0.030
656
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.029
657
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 55 0.029
658
c TBR024 Tuberous Sclerosis-1 50 0.029
659
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.029
660
ECT078 Ectodermal Dysplasia 2, Clouston Type 46 0.029
661
P NMN002 Niemann-Pick Disease 63 0.029
662
HYL004 Hyaline Fibromatosis Syndrome 38 0.029
663
KWS002 Kawasaki Disease 70 0.029
664
VHW001 Vohwinkel Syndrome 47 0.029
665
VRL011 Viral Infectious Disease 56 0.029
666
PPL049 Papillon-Lefevre Syndrome 45 0.029
667
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.029
668
ART001 Arterial Tortuosity Syndrome 51 0.029
669
NTR005 Nutritional Deficiency Disease 51 0.029
670
RCT018 Rectal Neoplasm 53 0.029
671
BRC012 Brucellosis 66 0.029
672
CLD014 Cole Disease 38 0.029
673
EPD033 Epidermolysis Bullosa, Lethal Acantholytic 34 0.029
674
P MCR010 Microcephaly 60 0.029
675
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 38 0.029
676
PRG004 Progeria 54 0.029
677
PRP082 Porphyria, Congenital Erythropoietic 44 0.029
678
MSL001 Measles 61 0.029
679
P PHT010 Photoparoxysmal Response 1 28 0.029
680
P FML012 Familial Partial Lipodystrophy 50 0.029
681
BZX001 Bazex Syndrome 38 0.029
682
OCL034 Oculocerebrocutaneous Syndrome 29 0.029
683
HYP074 Hypersensitivity Vasculitis 49 0.029
684
EPD040 Epidermolysis Bullosa Simplex with Pyloric Atresia 30 0.029
685
EPD045 Epidermolysis Bullosa, Junctional, with Pyloric Stenosis 37 0.029
686
P HYP098 Hypereosinophilic Syndrome 48 0.029
687
ADL030 Adult-Onset Still's Disease 57 0.029
688
P INT068 Intestinal Disease 60 0.029
689
HYP160 Hyperkeratosis Lenticularis Perstans 25 0.029
690
INF057 Inflammatory Linear Verrucous Epidermal Nevus 24 0.029
691
P THR014 Thrombocytopenia 63 0.029
692
ERY001 Erysipeloid 27 0.029
693
c PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 17 0.029
694
NRF007 Neurofibroma 53 0.029
695
SYR002 Syringocystadenoma Papilliferum 43 0.029
696
INT253 Intestinal Benign Neoplasm 48 0.029
697
TBR006 Tuberculoid Leprosy 44 0.029
698
TLN003 Telangiectasis 50 0.029
699
ADJ001 Adjustment Disorder 38 0.029
700
CHR463 Chronic Actinic Dermatitis 33 0.029
701
P LMY004 Leiomyosarcoma 54 0.029
702
ELP001 Elephantiasis 36 0.029
703
LKC003 Leukocyte Disease 45 0.029
704
HDN004 Head and Neck Carcinoma 54 0.029
705
DBT008 Diabetic Angiopathy 30 0.029
706
c CLR079 Colorectal Cancer 2 29 0.029
707
PMP009 Pemphigus Erythematosus 24 0.029
708
PRR013 Prurigo Nodularis 37 0.029
709
HYP266 Hypoxia 55 0.029
710
CRV038 Cervical Squamous Cell Carcinoma 58 0.029
711
OCC001 Occupational Dermatitis 32 0.029
712
MYC014 Mycobacterium Chelonae 32 0.029
713
EPT011 Epithelioid Leiomyosarcoma 39 0.029
714
BLD054 Blood Protein Disease 38 0.029
715
ATN004 Autonomic Neuropathy 44 0.029
716
IMP003 Impaired Renal Function Disease 36 0.029
717
c CHR090 Chronic Lymphocytic Leukemia 73 0.028
718
P ATX030 Ataxia-Telangiectasia 78 0.028
719
P OST005 Osteogenesis Imperfecta 68 0.028
720
P LVR013 Liver Disease 76 0.028
721
P OST012 Osteoarthritis 81 0.028
722
P KDN018 Kidney Disease 64 0.028
723
MRF001 Marfan Syndrome 73 0.028
724
P FCS002 Fucosidosis 57 0.028
725
P NRF002 Neurofibromatosis 66 0.028
726
P ALP004 Alport Syndrome 68 0.028
727
MCK007 Muckle-Wells Syndrome 62 0.028
728
CSY001 C Syndrome 49 0.028
729
CCC001 Coccidioidomycosis 55 0.028
730
MJD001 Majeed Syndrome 32 0.028
731
BHC003 Behcet Syndrome 60 0.028
732
c SBR001 Seborrheic Infantile Dermatitis 36 0.028
733
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 44 0.028
734
P WRD001 Waardenburg's Syndrome 56 0.028
735
PRC002 Paracoccidioidomycosis 57 0.028
736
c KRT055 Keratoderma, Palmoplantar, Punctate Type Ia 27 0.028
737
PRT036 Peritonitis 65 0.028
738
c ICH051 Ichthyosis, Congenital, Autosomal Recessive 11 27 0.028
739
CHR012 Chronic Granulomatous Disease 66 0.028
740
c CCK006 Cockayne Syndrome, Type B 37 0.028
741
c CCK005 Cockayne Syndrome, Type a 39 0.028
742
HPT074 Hepatic Adenoma, Somatic 35 0.028
743
P ORL007 Oral Cavity Cancer 58 0.028
744
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 34 0.028
745
OCL022 Ocular Melanoma 53 0.028
746
ACD009 Acid-Labile Subunit, Deficiency of 37 0.028
747
c CTS038 Cutis Laxa, Autosomal Recessive, Type Iia 27 0.028
748
SCL001 Scalp Dermatosis 19 0.028
749
TNG001 Tungiasis 38 0.028
750
TNC001 Tinea Cruris 30 0.028
751
PMP002 Pemphigoid Gestationis 35 0.028
752
FXF002 Fox-Fordyce Disease 37 0.028
753
CHL028 Childhood Type Dermatomyositis 40 0.028
754
FML039 Female Reproductive System Disease 49 0.028
755
ESN016 Eosinophilic Pustular Folliculitis 29 0.028
756
DNG002 Dengue Hemorrhagic Fever 60 0.028
757
FCL067 Focal Facial Dermal Dysplasia 1, Brauer Type 20 0.028
758
RMB001 Rombo Syndrome 19 0.028
759
P UVT001 Uveitis 60 0.028
760
HRP002 Herpes Gestationis 36 0.028
761
P TRT010 Teratoma 49 0.028
762
GDS001 Good Syndrome 46 0.028
763
RCT017 Rectal Disease 35 0.028
764
P LRY019 Laryngitis 55 0.028
765
c EFM001 Efemp2-Related Cutis Laxa 18 0.028
766
HYP458 Hyper Ige Syndrome 43 0.028
767
P INF049 Infantile Myofibromatosis 44 0.028
768
c CNN010 Connective Tissue Benign Neoplasm 31 0.028
769
OCH001 Ochronosis 33 0.028
770
FLL019 Follicular Mucinosis 35 0.028
771
LPS019 Lupus Erythematosus Tumidus 20 0.028
772
P MNC007 Monocytic Leukemia 52 0.028
773
SPN032 Spindle Cell Carcinoma 44 0.028
774
ADN013 Adenoid Squamous Cell Carcinoma 35 0.028
775
ALL007 Allergic Urticaria 31 0.028
776
LNT002 Lentigo Maligna Melanoma 35 0.028
777
MYC015 Mycobacterium Fortuitum 29 0.028
778
c ALD008 Aldh18a1-Related Cutis Laxa 16 0.028
779
P CRV039 Cervicitis 45 0.028
780
EPD052 Epidermolysis Bullosa Simplex Superficialis 21 0.028
781
c LTB003 Ltbp4-Related Cutis Laxa 14 0.028
782
c BSL027 Basal Cell Carcinoma 4 16 0.028
783
c BSL029 Basal Cell Carcinoma 6 17 0.028
784
PRK010 Porokeratosis of Mibelli 32 0.028
785
ELS003 Elastoderma 10 0.028
786
HMT018 Hematopoietic Stem Cell Transplantation 39 0.028
787
c PYC002 Pycr1-Related Cutis Laxa 11 0.028
788
CCT001 Cicatricial Ectropion 23 0.028
789
FBR019 Fibromatosis 40 0.028
790
MLG088 Malignant Germ Cell Tumor 27 0.028
791
c ELN002 Eln-Related Cutis Laxa 8 0.028
792
c FBL003 Fbln5-Related Cutis Laxa 17 0.028
793
P PNC035 Pancreatic Cancer 86 0.026
794
SMT004 Smith-Lemli-Opitz Syndrome 66 0.026
795
P HYP035 Hypophosphatasia 56 0.026
796
c SRC025 Sarcoidosis 1 58 0.026
797
WGN006 Wegener Granulomatosis 63 0.026
798
P SHR029 Short Syndrome 60 0.026
799
LPM004 Lipoma 59 0.026
800
c KRT056 Keratosis Palmoplantaris Striata I, Ad 21 0.026
801
HST011 Histoplasmosis 54 0.026
802
RBS003 Rabson-Mendenhall Syndrome 55 0.026
803
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.026
804
SVR004 Severe Combined Immunodeficiency 71 0.026
805
ALP001 Alopecia Universalis 57 0.026
806
EPD065 Epidermolytic Ichthyosis 38 0.026
807
SPT004 Septic Arthritis 60 0.026
808
NNT012 Neonatal Jaundice 49 0.026
809
CHL069 Cholesteatoma 51 0.026
810
P NTR004 Neutropenia 59 0.026
811
ACR002 Acrocapitofemoral Dysplasia 35 0.026
812
P MCP010 Mucopolysaccharidosis 58 0.026
813
P BRN009 Burning Mouth Syndrome 54 0.026
814
P CRD011 Cardiomyopathy 66 0.026
815
P CND004 Candidiasis 58 0.026
816
c EHL028 Ehlers-Danlos Syndrome, Type Viii 26 0.026
817
GYN001 Gynecomastia 49 0.026
818
c VRL010 Viral Hepatitis 60 0.026
819
c EPD043 Epidermolysis Bullosa Dystrophica, Ad 21 0.026
820
LBM003 Lobomycosis 31 0.026
821
PLM135 Palmoplantar Keratoderma, Bothnian Type 22 0.026
822
MXD005 Mixed Connective Tissue Disease 63 0.026
823
HPR003 Heparin-Induced Thrombocytopenia 45 0.026
824
TNP002 Tinea Profunda 27 0.026
825
DFF001 Diffuse Cutaneous Mastocytosis 42 0.026
826
c AST039 Asthma 2 28 0.026
827
MLR002 Miliary Tuberculosis 39 0.026
828
c JVN003 Juvenile Xanthogranuloma 41 0.026
829
SCL025 Scleromyxedema 33 0.026
830
c DRM040 Dermatitis Herpetiformis, Familial 18 0.026
831
XNT003 Xanthomatosis 45 0.026
832
PRP021 Peripheral Nervous System Neoplasm 49 0.026
833
NCR007 Necrotizing Fasciitis 43 0.026
834
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 50 0.026
835
GNT018 Gianotti Crosti Syndrome 23 0.026
836
MCR088 Microscopic Polyangiitis 47 0.026
837
CRN024 Corneal Disease 45 0.026
838
PSD078 Pseudofolliculitis Barbae 20 0.026
839
PLM014 Pleomorphic Adenoma 51 0.026
840
ACT167 Acute Generalized Exanthematous Pustulosis 39 0.026
841
FCT008 Factitious Disorder 42 0.026
842
P ATX004 Ataxia 53 0.026
843
ATY008 Atypical Lipomatous Tumor 39 0.026
844
INT104 Intravascular Papillary Endothelial Hyperplasia 34 0.026
845
EGG001 Egg Allergy 44 0.026
846
PRL042 Proliferating Trichilemmal Cyst 33 0.026
847
EPT020 Epithelioid Hemangioendothelioma 46 0.026
848
PRV003 Perivascular Epithelioid Cell Tumor 38 0.026
849
CHR008 Choroiditis 43 0.026
850
SPR005 Superficial Basal Cell Carcinoma 37 0.026
851
P CHR345 Chronic Pain 45 0.026
852
NVS007 Nevus of Ota 20 0.026
853
FBR054 Fibroma 44 0.026
854
XRD026 Xeroderma Pigmentosum-Cockayne Syndrome Complex 32 0.026
855
ERS002 Erosive Pustular Dermatosis of the Scalp 20 0.026
856
BND014 Bone Development Disease 40 0.026
857
P PST059 Pustular Psoriasis 33 0.026
858
MSC004 Muscle Tissue Disease 35 0.026
859
VSC047 Vascular Malformation 45 0.026
860
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.025
861
P PRS040 Prostate Cancer 89 0.025
862
P LNG032 Lung Cancer 92 0.025
863
ANX002 Anxiety Disorder 67 0.025
864
KRT004 Keratitis 70 0.025
865
PRP032 Porphyria Variegata 51 0.025
866
CPR001 Coproporphyria 54 0.025
867
ACR007 Acromegaly 66 0.025
868
P ERY008 Erythromelalgia 50 0.025
869
INS024 Insulin-Like Growth Factor I 75 0.025
870
P TMP003 Temporal Arteritis 61 0.025
871
c ALB010 Albinism, Oculocutaneous, Type Ib 35 0.025
872
ANT024 Anthrax Disease 50 0.025
873
c CNG401 Congenital Heart Disease 67 0.025
874
c CHR089 Chronic Kidney Failure 67 0.025
875
NRC019 Neurocutaneous Melanosis, Somatic 38 0.025
876
P ASP006 Aspergillosis 61 0.025
877
URN009 Urinary System Disease 52 0.025
878
PTC001 Potocki-Shaffer Syndrome 37 0.025
879
STR008 Strongyloidiasis 51 0.025
880
EPD031 Epidermolysis Bullosa Simplex, Ogna Type 22 0.025
881
EPD034 Epidermolysis Bullosa, Pretibial 30 0.025
882
SLP005 Sleep Disorder 52 0.025
883
ADP001 Adiposis Dolorosa 44 0.025
884
SCR002 Scurvy 47 0.025
885
SCH014 Schistosomiasis 59 0.025
886
EPD041 Epidermolysis Bullosa Simplex, Weber-Cockayne Type 38 0.025
887
SCH038 Schopf-Schulz-Passarge Syndrome 28 0.025
888
P MNN013 Meningitis 66 0.025
889
DRC001 Dracunculiasis 38 0.025
890
MVM001 Movement Disease 45 0.025
891
EPD057 Epidermylysis Bullosa Simplex-Mcr 21 0.025
892
HYP022 Hypohidrosis 41 0.025
893
P ESP024 Esophagitis 62 0.025
894
P ANT006 Antiphospholipid Syndrome 60 0.025
895
c ATM011 Autoimmune Hepatitis 62 0.025
896
LNG099 Lung Disease 63 0.025
897
P WLL010 Woolly Hair Syndrome 33 0.025
898
P PLM036 Pulmonary Fibrosis 69 0.025
899
OST017 Osteomyelitis 60 0.025
900
EHL060 Ehlers-Danlos Syndrome Due to Tenascin X Deficiency 29 0.025
901
ELS002 Elastosis Perforans Serpiginosa 30 0.025
902
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 32 0.025
903
P ANG015 Angioedema 53 0.025
904
c EHL065 Ehlers-Danlos Syndrome, Type V 20 0.025
905
P LPC002 Lip Cancer 50 0.025
906
OCL020 Ocular Cicatricial Pemphigoid 51 0.025
907
P MSC033 Muscle Disorders 52 0.025
908
BRD005 Borderline Leprosy 31 0.025
909
c PMP006 Pemphigus Vulgaris, Familial 16 0.025
910
GRW032 Growth Factors, Combined Defect of 23 0.025
911
MCR103 Microtia 37 0.025
912
LNR006 Linear Iga Disease 40 0.025
913
INF034 Infective Endocarditis 50 0.025
914
MYP002 Myoepithelial Carcinoma 38 0.025
915
BDY001 Body Dysmorphic Disorder 41 0.025
916
VGN020 Vaginal Disease 42 0.025
917
SWT003 Sweat Gland Disease 33 0.025
918
QNQ001 Quinquaud's Decalvans Folliculitis 16 0.025
919
KRT044 Keratosis Pilaris 26 0.025
920
GRN022 Granulosa Cell Tumor of the Ovary 39 0.025
921
CMM003 Common Wart 41 0.025
922
GLM008 Glomus Tumor 41 0.025
923
P CNN004 Connective Tissue Cancer 44 0.025
924
FML037 Female Breast Cancer 49 0.025
925
VLV044 Vulvar Intraepithelial Neoplasia 44 0.025
926
LCH013 Lichen Planus Pemphigoides 28 0.025
927
PRP036 Peripheral T-Cell Lymphoma 44 0.025
928
c INS002 in Situ Carcinoma 51 0.025
929
EXT052 Extraskeletal Ewing Sarcoma 33 0.025
930
ATM053 Autoimmune Disease 2 16 0.025
931
DND018 Dendritic Cell Tumor 40 0.025
932
HNS001 Hansen's Disease 30 0.025
933
P CYS017 Cystic Teratoma 40 0.025
934
DRM003 Dermatosis Papulosa Nigra 32 0.025
935
RTN023 Retinitis 49 0.025
936
c RTH004 Rothmund-Thomson Syndrome Type 1 13 0.025
937
BCK006 Back Pain 40 0.025
938
ANG037 Angiomatosis 33 0.025
939
PNC085 Penicillin Allergy 41 0.025
940
URM005 Uremic Pruritus 38 0.025
941
DYS133 Dyschromatosis Universalis 21 0.025
942
LNR009 Linear Atrophoderma of Moulin 11 0.025
943
ATM012 Autoimmune Disease of Blood 36 0.025
944
CTN031 Cutaneous Pseudolymphoma 14 0.025
945
GST078 Gastrointestinal Allergy 41 0.025
946
c CYP003 Cyp4f22-Related Autosomal Recessive Congenital Ichthyosis 7 0.025
947
c ALX004 Alox12b-Related Autosomal Recessive Congenital Ichthyosis 7 0.025
948
c ALX005 Aloxe3-Related Autosomal Recessive Congenital Ichthyosis 7 0.025
949
c ABC002 Abca12-Related Autosomal Recessive Congenital Ichthyosis 8 0.025
950
c PNP002 Pnpla1-Related Autosomal Recessive Congenital Ichthyosis 7 0.025
951
c TGM001 Tgm1-Related Autosomal Recessive Congenital Ichthyosis 7 0.025
952
HPT023 Hepatocellular Carcinoma 90 0.024
953
P MTC003 Metachromatic Leukodystrophy 71 0.024
954
ALK013 Alkaptonuria 54 0.024
955
WLL001 Williams-Beuren Syndrome 61 0.024
956
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.024
957
P WSK001 Wiskott-Aldrich Syndrome 70 0.024
958
OSS012 Osseous Heteroplasia, Progressive 35 0.024
959
CHD001 Chediak-Higashi Syndrome 66 0.024
960
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.024
961
PRT093 Proteus Syndrome, Somatic 54 0.024
962
OCC006 Occipital Horn Syndrome 47 0.024
963
HRT031 Hartnup Disorder 45 0.024
964
P URF003 Urofacial Syndrome 1 51 0.024
965
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 40 0.024
966
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 52 0.024
967
WRD025 Waardenburg Syndrome, Type 2e, with or Without Neurologic Involvement 43 0.024
968
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 30 0.024
969
c NRF018 Neurofibromatosis, Type 1 69 0.024
970
c CTS023 Cutis Laxa, Autosomal Recessive, Type Iib 28 0.024
971
HMF006 Hemifacial Microsomia 54 0.024
972
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 27 0.024
973
P HYP086 Hypothyroidism 63 0.024
974
BRT002 Birt-Hogg-Dube Syndrome 51 0.024
975
SPN180 Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like 26 0.024
976
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 36 0.024
977
P PLY017 Polyarteritis Nodosa 54 0.024
978
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.024
979
c XRD018 Xeroderma Pigmentosum, Group a 49 0.024
980
c HPT073 Hepatitis C Virus 72 0.024
981
P PNL012 Penile Cancer 54 0.024
982
OLM001 Olmsted Syndrome 33 0.024
983
RTC008 Reticulate Acropigmentation of Kitamura 36 0.024
984
P LKD001 Leukodystrophy 58 0.024
985
DYS022 Dyschromatosis Symmetrica Hereditaria 47 0.024
986
c MLN032 Melanoma, Cutaneous Malignant, 2 36 0.024
987
BNC003 Bone Cancer 44 0.024
988
ODN009 Odontoonychodermal Dysplasia 25 0.024
989
SPN041 Spinal Cord Disease 50 0.024
990
RHM001 Rheumatic Fever 50 0.024
991
VBR001 Vibratory Urticaria 21 0.024
992
PRT058 Pure Autonomic Failure 47 0.024
993
P GST049 Gastrointestinal System Cancer 59 0.024
994
HYW001 Hay-Wells Syndrome 33 0.024
995
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.024
996
P PNC044 Pancreatitis 62 0.024
997
STM006 Stomach Disease 48 0.024
998
P MSC007 Muscle Hypertrophy 55 0.024
999
c CTS008 Cutis Laxa, Autosomal Dominant 33 0.024
1000
ERD001 Erdheim-Chester Disease 51 0.024
1001
CLD011 Cold Urticaria 36 0.024
1002
DRM008 Dermatographia 30 0.024
1003
RLP001 Relapsing Polychondritis 52 0.024
1004
c APL023 Aplasia Cutis Congenita, Nonsyndromic 24 0.024
1005
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 30 0.024
1006
c CLR085 Colorectal Cancer 1 39 0.024
1007
c FCL046 Focal Facial Dermal Dysplasia 4 16 0.024
1008
TNM002 Tinea Manuum 23 0.024
1009
RCS008 Recessive Dystrophic Epidermolysis Bullosa-Generalized Other 20 0.024
1010
c PSR019 Psoriasis Susceptibility 13 24 0.024
1011
BRN121 Branchiootorenal/branchiootic Syndrome 17 0.024
1012
MNN017 Mononeuropathy 37 0.024
1013
PRK076 Porokeratosis 2, Palmar, Plantar, and Disseminated Type 14 0.024
1014
SXL003 Sexual Disorder 45 0.024
1015
CPL005 Capillary Disease 39 0.024
1016
ACN001 Acinar Cell Carcinoma 48 0.024
1017
LYM051 Lymphomatoid Granulomatosis 46 0.024
1018
TRT003 Tertiary Syphilis 33 0.024
1019
CLF001 Cleft Lip 48 0.024
1020
ATR020 Atrophoderma of Pierini and Pasini 8 0.024
1021
P LPD010 Lipodystrophy 51 0.024
1022
DRM013 Dermoid Cyst 39 0.024
1023
c DMN009 Dominant Ichthyosis Vulgaris 14 0.024
1024
GTT002 Guttate Psoriasis 31 0.024
1025
CWP001 Cowpox 45 0.024
1026
ACN010 Acanthoma 29 0.024
1027
ANC002 Anca-Associated Vasculitis 43 0.024
1028
MYC017 Mycobacterium Kansasii 40 0.024
1029
TTR011 Tetraploidy 41 0.024
1030
ECT004 Ecthyma 37 0.024
1031
HDN002 Head Injury 47 0.024
1032
LCH004 Lichen Disease 37 0.024
1033
P PRM145 Primary Anetoderma 19 0.024
1034
P PRN022 Perineurioma 37 0.024
1035
ARG004 Argyria 20 0.024
1036
BSL006 Basaloid Squamous Cell Carcinoma 40 0.024
1037
BLL015 Bullous Lichen Planus 18 0.024
1038
ALX002 Alexithymia 37 0.024
1039
HMN016 Hemangioendothelioma 40 0.024
1040
RHB007 Rhabdomyomatous Mesenchymal Hamartoma 12 0.024
1041
GRN003 Granulomatous Dermatitis 32 0.024
1042
CRT049 Critical Limb Ischemia 51 0.024
1043
CRY006 Cryofibrinogenemia 25 0.024
1044
BTL002 Beta-Lactam Allergy 36 0.024
1045
c CLL012 Cell Type Benign Neoplasm 41 0.024
1046
ORL022 Oral Erosive Lichen 33 0.024
1047
LMB062 Limb Ischemia 48 0.024
1048
MLN013 Melanoma Metastasis 35 0.024
1049
MLR004 Malaria 80 0.023
1050
HDG012 Hodgkin Lymphoma 75 0.023
1051
c SPN225 Spondyloarthropathy 1 62 0.023
1052
P SJG002 Sjogren-Larsson Syndrome 51 0.023
1053
P AGM005 Agammaglobulinemia, X-Linked 1 60 0.023
1054
P THN009 Thanatophoric Dysplasia, Type I 62 0.023
1055
AND015 Androgen Insensitivity 64 0.023
1056
P CWD001 Cowden Disease 63 0.023
1057
CRH001 Crohn's Disease 76 0.023
1058
c CWD006 Cowden Syndrome 1 43 0.023
1059
c INF071 Inflammatory Bowel Disease 1 51 0.023