Search results for "skin"

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

5417 hits were found for 'skin'

# Family MCID Name MIFTS Score
1
c PLN018 Peeling Skin Syndrome 2 40 4.010
2
P PLN008 Peeling Skin Syndrome 45 3.697
3
c LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 37 3.536
4
SKN016 Skin Disease 66 3.334
5
P ECT007 Ectodermal Dysplasia/skin Fragility Syndrome 42 3.144
6
c PLN017 Peeling Skin Syndrome 1 34 3.131
7
c PLN021 Peeling Skin Syndrome 3 29 2.976
8
STF002 Stiff Skin Syndrome 53 2.878
9
P SKN013 Skin Benign Neoplasm 43 2.866
10
WRN004 Wrinkly Skin Syndrome 32 2.846
11
SKN023 Skin Tag 44 2.605
12
SKN024 Skin Fragility-Woolly Hair Syndrome 19 2.490
13
SKN019 Skin Melanoma 62 2.483
14
SKN020 Skin Papilloma 30 2.362
15
SKN018 Skin Hemangioma 39 2.333
16
GRN032 Granulomatous Slack Skin Disease 19 2.324
17
RTT001 Ritter's Disease 40 2.321
18
P RST011 Restrictive Dermopathy, Lethal 41 2.319
19
PRN056 Parana Hard-Skin Syndrome 14 2.311
20
P SKN063 Skin Creases, Congenital Symmetric Circumferential, 1 18 2.299
21
SKN022 Skin Squamous Cell Carcinoma 41 2.241
22
SKN005 Skin Atrophy 40 2.187
23
BRB006 Barber-Say Syndrome 33 2.123
24
HYP346 Hypotrichosis and Recurrent Skin Vesicles 17 2.106
25
PLM082 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal 18 2.104
26
CHR100 Chronic Ulcer of Skin 40 1.922
27
BLL007 Bullous Skin Disease 38 1.920
28
c SKN012 Skin Carcinoma in Situ 38 1.916
29
VSC012 Vesiculobullous Skin Disease 36 1.898
30
P GNR027 Generalized Peeling Skin Syndrome 19 1.898
31
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 1.890
32
NDL009 Nodular Basal Cell Carcinoma 31 1.890
33
SKN001 Skin Angiosarcoma 13 1.890
34
PLN020 Peeling Skin with Leukonychia, Acral Punctate Keratoses, Cheilitis, and Knuckle Pads 16 1.886
35
SRC008 Sarcomatoid Squamous Cell Skin Carcinoma 26 1.884
36
c INF144 Inflammatory Skin and Bowel Disease, Neonatal, 1 20 1.884
37
c LNR014 Linear Skin Defects with Multiple Congenital Anomalies 3 18 1.884
38
c INF146 Inflammatory Skin and Bowel Disease, Neonatal, 2 17 1.884
39
MLG007 Malignant Skin Fibrous Histiocytoma 30 1.876
40
SKN061 Skin Fragility-Woolly Hair-Palmoplantar Keratoderma Syndrome 11 1.876
41
SKN002 Skin Lipoma 25 1.874
42
SKN011 Skin Pilomatrix Carcinoma 21 1.874
43
SKN008 Skin Glomus Tumor 11 1.874
44
MTT001 Metatypical Basal Cell Carcinoma 17 1.871
45
SQM006 Squamous Cell Carcinoma 70 1.870
46
EPD010 Epidermal Appendage Tumor 16 1.868
47
VSC009 Vascular Skin Disease 19 1.720
48
UVN001 Uv-Induced Skin Damage 20 1.665
49
JSS001 Jessner's Lymphocytic Infiltration of the Skin 13 1.655
50
SKN027 Skin Conditions 43 1.652
51
ANG016 Angiokeratoma 40 1.649
52
SKN021 Skin Sarcoma 25 1.643
53
CLF045 Cleft, Median, of Upper Lip with Polyps of Facial Skin and Nasal Mucosa 19 1.641
54
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 34 1.639
55
P LNR015 Linear Skin Defects with Multiple Congenital Anomalies 27 1.639
56
SQM001 Squamous Cell Papilloma of Skin 12 1.637
57
CTN004 Cutaneous Fibrous Histiocytoma 41 1.631
58
VRR003 Verruciform Xanthoma of Skin 19 1.631
59
SDD003 Saddan 30 1.629
60
SKN010 Skin Epithelioid Hemangioma 15 1.629
61
P SKN009 Skin Granular Cell Tumor 14 1.629
62
CLR010 Clear Cell Squamous Cell Skin Carcinoma 11 1.629
63
CTN002 Cutaneous Mucoepidermoid Carcinoma 23 1.626
64
c MLG050 Malignant Granular Cell Skin Tumor 11 1.626
65
DRM002 Dermoid Cyst of Skin 11 1.626
66
SKN017 Skin Glomangioma 9 1.626
67
BSL002 Basaloid Squamous Cell Skin Carcinoma 7 1.626
68
ECC006 Eccrine Mixed Tumor of Skin 7 1.626
69
ACN008 Acantholytic Squamous Cell Skin Carcinoma 6 1.626
70
ADR038 Adermatoglyphia 46 1.420
71
P EHL001 Ehlers-Danlos Syndrome 63 1.404
72
KPS004 Kaposi Sarcoma 67 1.376
73
ATM016 Autoimmune Disease of Skin and Connective Tissue 29 1.361
74
SKN006 Skin Sarcoidosis 33 1.359
75
KWS001 Kwashiorkor 40 1.351
76
NRT002 Neurotic Excoriation 30 1.351
77
MCR095 Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 28 1.351
78
MLT104 Multiple Benign Circumferential Skin Creases on Limbs 21 1.351
79
P CPL006 Capillary Hemangioma 51 1.348
80
DYS044 Dysmorphism Cleft Palate Loose Skin 10 1.346
81
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 35 1.343
82
CTN013 Cutaneous Anthrax 34 1.343
83
P NNT037 Neonatal Inflammatory Skin and Bowel Disease 22 1.343
84
ECC004 Eccrine Porocarcinoma 36 1.341
85
EYB005 Eyebrows, Duplication of, with Stretchable Skin and Syndactyly 12 1.341
86
c ALB017 Albinism, Oculocutaneous, Type Vi 28 1.338
87
c SKN062 Skin Creases, Congenital Symmetric Circumferential, 2 14 1.338
88
RDS002 Red Skin Pigment Anomaly of New Guinea 6 1.338
89
LYM008 Lymphangiosarcoma 47 1.335
90
CTN009 Cutaneous Adenocystic Carcinoma 31 1.335
91
ECC008 Eccrine Sweat Gland Neoplasm 28 1.335
92
c GNR024 Generalized Peeling Skin Syndrome Type C 12 1.335
93
c SPN111 Spinocerebellar Ataxia Autosomal Recessive 5 25 1.332
94
MNT259 Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies 14 1.332
95
SKN007 Skin Meningioma 11 1.332
96
CND003 Candidal Paronychia 10 1.332
97
PRN012 Perianal Skin Paget's Disease 7 1.332
98
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 6 1.332
99
SKN004 Skin Amelanotic Melanoma 6 1.332
100
PLN004 Plantar Verrucous Skin Carcinoma 5 1.332
101
WND001 Wound Botulism 31 1.329
102
CLR015 Clear Cell Basal Cell Carcinoma 25 1.329
103
CTN010 Cutaneous Ganglioneuroma 24 1.329
104
SGN001 Signet Ring Basal Cell Carcinoma 8 1.329
105
CRS012 Carasil Syndrome 29 1.325
106
CTN001 Cutaneous Solitary Mastocytoma 27 1.325
107
ADM002 Adamantinoid Basal Cell Epithelioma 10 1.325
108
SRC003 Sarcomatoid Basal Cell Carcinoma 10 1.325
109
DRM006 Dermatitis 66 1.280
110
c BSL007 Basal Cell Carcinoma 65 1.133
111
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 1.047
112
c DWL002 Dowling-Degos Disease 1 49 1.042
113
P CTS001 Cutis Laxa 58 1.039
114
P DRM010 Dermatomyositis 62 1.035
115
PGM003 Pigmentation Disease 39 1.032
116
PMS001 Poems Syndrome 52 1.010
117
CNG008 Congenital Ichthyosiform Erythroderma 56 0.991
118
P APL006 Aplasia Cutis Congenita 52 0.991
119
ACR014 Acral Lentiginous Melanoma 45 0.987
120
P FNC043 Fanconi Anemia, Complementation Group E 55 0.984
121
EPD053 Epidermal Nevus, Somatic 53 0.984
122
P SBR004 Seborrheic Dermatitis 39 0.984
123
HDR004 Hidradenoma 32 0.982
124
GNT020 Giant Congenital Nevus 27 0.982
125
P ANG013 Angioma Serpiginosum 31 0.978
126
MLT122 Multiple Self-Healing Squamous Epithelioma, Susceptiblity to 25 0.978
127
MCH008 Michelin Tire Baby Syndrome 13 0.978
128
BLM001 Bloom Syndrome 63 0.976
129
BRK001 Brooke-Spiegler Syndrome 48 0.976
130
CHN002 Chancroid 37 0.972
131
KRT013 Keratolytic Winter Erythema 24 0.972
132
P CRN038 Carney Complex Variant 53 0.970
133
PSD101 Pseudoxanthoma Elasticum-Like Skin Manifestations with Retinitis Pigmentosa 12 0.970
134
AML001 Amelanotic Melanoma 40 0.967
135
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 35 0.967
136
P SPR013 Spiradenoma 36 0.965
137
PGT003 Paget Disease, Extramammary 34 0.965
138
ADN015 Adenoid Basal Cell Carcinoma 34 0.965
139
CTN027 Cutaneous Mastocytoma 24 0.965
140
MCC010 Mccune-Albright Syndrome, Somatic, Mosaic 58 0.962
141
HYP691 Hypomelanosis of Ito 42 0.962
142
ESN002 Eosinophilia-Myalgia Syndrome 42 0.962
143
EXF006 Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-Like 19 0.962
144
c PLL014 Pellagra-Like Syndrome 17 0.962
145
KSK002 Kosaki Overgrowth Syndrome 17 0.962
146
DRM042 Dermatoosteolysis, Kirghizian Type 15 0.962
147
SPR107 Sparse Hair-Short Stature-Skin Anomalies Syndrome 8 0.962
148
c GRS013 Griscelli Syndrome, Type 1 47 0.959
149
c MLG049 Malignant Syringoma 23 0.959
150
PSD059 Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency 23 0.959
151
MCR036 Macroepiphyseal Dysplasia with Osteoporosis, Wrinkled Skin, and Aged Appearance 8 0.959
152
P MLN043 Melanoma, Cutaneous Malignant 8 37 0.957
153
EBD002 Ebd, Bart Type 12 0.957
154
NXS001 Naxos Disease 46 0.953
155
c MCL040 Macular Degeneration, Age-Related, 3 33 0.953
156
SNL003 Senile Angioma 33 0.953
157
NGL001 Naegeli-Franceschetti-Jadassohn Syndrome 31 0.953
158
CYS004 Cystic Basal Cell Carcinoma 28 0.953
159
MCR274 Microcephalic Primordial Dwarfism, Montreal Type 17 0.953
160
FLY003 Flynn-Aird Syndrome 17 0.953
161
HLL006 Halal Setton Wang Syndrome 13 0.953
162
BRS103 Bier Spots 12 0.953
163
PLM113 Palmoplantar Keratoderma-Sclerodactyly Syndrome 9 0.953
164
c DSP002 Dsp-Related Ectodermal Dysplasia/skin Fragility Syndrome 6 0.953
165
c PKP001 Pkp1-Related Ectodermal Dysplasia/skin Fragility Syndrome 6 0.953
166
PGM025 Pigmentation Defects-Palmoplantar Keratoderma-Skin Carcinoma Syndrome 5 0.953
167
ICH027 Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 5 0.953
168
HRD105 Hereditary Sensorimotor Neuropathy with Hyperelastic Skin 4 0.953
169
MNT019 Mental Retardation Hypotonia Skin Hyperpigmentation 3 0.953
170
SHR013 Short Stature Abnormal Skin Pigmentation Mental Retardation 3 0.953
171
MSM009 Mesomelic Dysplasia Skin Dimples 3 0.953
172
CTN012 Cutaneous Leiomyosarcoma 33 0.950
173
SBC009 Sebaceous Adenoma 33 0.950
174
CMB022 Combined Cellular and Humoral Immune Defects with Granulomas 31 0.950
175
PGM002 Pigmented Basal Cell Carcinoma 28 0.950
176
INF027 Infiltrative Basal Cell Carcinoma 28 0.950
177
ANG065 Angioma, Tufted 26 0.950
178
HDR001 Hidrocystoma 24 0.950
179
ANL016 Anal Margin Carcinoma 20 0.950
180
ECC001 Eccrine Papillary Adenocarcinoma 19 0.950
181
FCL068 Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome 19 0.950
182
c MLG048 Malignant Acrospiroma 17 0.950
183
INT287 Intellectual Disability-Hypotonia-Skin Hyperpigmentation Syndrome 10 0.950
184
SKN026 Skin Cancer, Non Melanoma, Childhood 8 0.950
185
END012 Endometriosis in Scar of Skin 8 0.950
186
SKL025 Skeletal Overgrowth-Craniofacial Dysmorphism-Hyperelastic Skin-White Matter Lesions Syndrome 7 0.950
187
GLL032 Galloway-Mowat Syndrome 51 0.946
188
INF028 Infundibulocystic Basal Cell Carcinoma 27 0.946
189
SPR033 Superficial Spreading Melanoma 18 0.946
190
TNL002 Toenail Dystrophy, Isolated 18 0.946
191
CRN070 Corneodermatoosseous Syndrome 16 0.946
192
CTN008 Cutaneous Liposarcoma 12 0.946
193
NVF002 Nevi Flammei 11 0.946
194
ANG030 Angiomatosis, Diffuse Corticomeningeal, of Divry and Van Bogaert 8 0.946
195
c LTH013 Lethal Restrictive Dermopathy, Lmna-Related 7 0.946
196
c LTH014 Lethal Restrictive Dermopathy, Zmpste24-Related 7 0.946
197
SBC013 Sebaceous Basal Cell Carcinoma 7 0.946
198
P APL009 Aplasia Cutis Congenita of Limbs Recessive 7 0.946
199
RYM001 Roy Maroteaux Kremp Syndrome 7 0.946
200
SQR001 Sequeiros Sack Syndrome 6 0.946
201
LMY001 Leiomyoma Cutis 24 0.942
202
ECC002 Eccrine Acrospiroma 21 0.942
203
CPL002 Capillary Lymphangioma 18 0.942
204
MLT066 Multiple Cutaneous and Uterine Leiomyomas 17 0.942
205
ANL007 Anal Margin Squamous Cell Carcinoma 14 0.942
206
ECC003 Eccrine Papillary Adenoma 12 0.942
207
ANL013 Anal Margin Basal Cell Carcinoma 12 0.942
208
MCR016 Micronodular Basal Cell Carcinoma 11 0.942
209
BNG008 Benign Dermal Neurilemmoma 10 0.942
210
ALG003 Al Gazali Aziz Salem Syndrome 9 0.942
211
DNT019 Daentl Towsend Siegel Syndrome 9 0.942
212
THM006 Thumb Deformity, Alopecia, Pigmentation Anomaly 7 0.942
213
JNS005 Jones Hersh Yusk Syndrome 7 0.942
214
HRY007 Hairy Palms and Soles 7 0.942
215
DRM001 Dermal Unilateral Segmental Cavernous Angioma 6 0.942
216
MST010 Mastocytosis Cutaneous with Short Stature Conductive Hearing Loss and Microtia 6 0.942
217
GRB001 Grubben De Cock Borghgraef Syndrome 6 0.942
218
TNG005 Tang Hsi Ryu Syndrome 6 0.942
219
JDG001 Judge Misch Wright Syndrome 5 0.942
220
BDH001 Boudhina Yedes Khiari Syndrome 5 0.942
221
MLN017 Milner Khallouf Gibson Syndrome 4 0.942
222
RVL001 Ruvalcaba Churesigaew Myhre Syndrome 4 0.942
223
ELL003 Elliott Ludman Teebi Syndrome 4 0.942
224
MGR004 Megarbane Jalkh Syndrome 4 0.942
225
MLN008 Melanoma 62 0.184
226
P ATP001 Atopic Dermatitis 62 0.146
227
P PSR002 Psoriasis 61 0.142
228
BRN106 Burns 52 0.120
229
P LYM118 Lymphoma 69 0.112
230
CTN007 Cutaneous Leishmaniasis 62 0.112
231
ADM013 Adamantinoma of Long Bones 57 0.111
232
KRT009 Keratosis 52 0.096
233
ACT008 Actinic Keratosis 51 0.092
234
AYM001 Ayme-Gripp Syndrome 41 0.091
235
ACN011 Acne 62 0.090
236
EPD016 Epidermolysis Bullosa 57 0.088
237
ATP002 Atopy 66 0.085
238
ALL026 Allergic Hypersensitivity Disease 52 0.084
239
CNT047 Contact Dermatitis 61 0.084
240
P LPS004 Lupus Erythematosus 64 0.081
241
MYC006 Mycosis Fungoides 66 0.079
242
PRM025 Primary Bacterial Infectious Disease 41 0.079
243
URT039 Urticaria 57 0.078
244
WRN005 Wrinkles 37 0.078
245
TBR010 Tuberculosis 70 0.073
246
P EXN002 Exanthem 57 0.073
247
CLL003 Cellulitis 51 0.073
248
PMP001 Pemphigus 50 0.073
249
P NRP001 Neuropathy 59 0.071
250
CNN005 Connective Tissue Disease 62 0.070
251
P ART022 Arthritis 75 0.070
252
P LPR003 Leprosy 69 0.069
253
P LKM002 Leukemia 71 0.069
254
BLL006 Bullous Pemphigoid 59 0.068
255
ALL010 Allergic Contact Dermatitis 57 0.066
256
RSC001 Rosacea 52 0.066
257
END072 Endotheliitis 42 0.066
258
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.066
259
P ICH004 Ichthyosis 52 0.065
260
EPD001 Epidermodysplasia Verruciformis 50 0.063
261
P BRS047 Breast Cancer 100 0.062
262
P CTN015 Cutaneous T Cell Lymphoma 50 0.062
263
PPL022 Papilloma 55 0.061
264
IMP004 Impetigo 42 0.061
265
PLM102 Palmoplantar Keratoderma, Epidermolytic 47 0.061
266
BRN105 Burn Scar 37 0.061
267
P SYS005 Systemic Scleroderma 61 0.060
268
CLV009 Clove Syndrome, Somatic 41 0.059
269
MRK001 Merkel Cell Carcinoma 52 0.059
270
FCL001 Facial Dermatosis 23 0.059
271
P DRM007 Dermatitis Herpetiformis 51 0.058
272
P PSD087 Pseudoxanthoma Elasticum 66 0.056
273
c LCL006 Localized Scleroderma 61 0.056
274
P SYN001 Syndactyly 53 0.056
275
IMM136 Immune System Disease 51 0.056
276
C3D001 C3 Deficiency 53 0.056
277
MCR013 Microphthalmia 60 0.055
278
P KRT005 Keratoacanthoma 46 0.055
279
KLD001 Keloids 51 0.055
280
SRC014 Sarcoma 66 0.054
281
P NRV006 Nervous System Cancer 60 0.054
282
P PMP005 Pemphigus Vulgaris 51 0.054
283
ALP008 Alopecia 57 0.054
284
P INF032 Infertility 59 0.053
285
NTH001 Netherton Syndrome 54 0.053
286
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.052
287
P PLY019 Polyneuropathy 56 0.052
288
LYM006 Lymphoepithelioma-Like Carcinoma 43 0.052
289
P AST005 Asthma 82 0.051
290
MLG108 Malignant Melanoma, Somatic 60 0.051
291
P HMN010 Hemangioma 59 0.051
292
CRC006 Carcinoid Syndrome 52 0.051
293
c BSL024 Basal Cell Carcinoma 1 42 0.051
294
PSR001 Psoriatic Arthritis 64 0.050
295
DBT062 Diabetic Foot Ulcers 51 0.050
296
HDR002 Hidradenitis Suppurativa 51 0.050
297
EPD006 Epidermolysis Bullosa Acquisita 45 0.050
298
HYP457 Hypertrophic Scars 45 0.050
299
c CHR579 Chiari Malformation Type Ii 37 0.050
300
P THY032 Thyroiditis 54 0.050
301
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 54 0.050
302
ECT006 Ectodermal Dysplasia 52 0.050
303
PYD001 Pyoderma Gangrenosum 51 0.050
304
SCB001 Scabies 47 0.050
305
c BSL025 Basal Cell Carcinoma 2 17 0.050
306
P HRP006 Herpes Simplex 65 0.049
307
P MST009 Mastocytosis 56 0.049
308
PYD002 Pyoderma 48 0.049
309
c PRM023 Pre-Malignant Neoplasm 41 0.049
310
P MDL005 Medulloblastoma 77 0.049
311
LSH001 Leishmaniasis 66 0.049
312
DRM014 Dermatofibrosarcoma Protuberans 61 0.049
313
P RHN004 Rhinitis 60 0.049
314
INC021 Incontinentia Pigmenti 59 0.049
315
IRR003 Irritant Dermatitis 44 0.049
316
VSC011 Vasculitis 62 0.048
317
WLL006 Wells Syndrome 59 0.048
318
KND001 Kindler Syndrome 57 0.048
319
c PND001 Pain Disorder 54 0.048
320
TST021 Testicular Germ Cell Tumor 69 0.047
321
P HPT021 Hepatitis 69 0.047
322
EWN003 Ewing Sarcoma 66 0.047
323
P BCL006 B-Cell Lymphomas 65 0.047
324
P PRP003 Porphyria Cutanea Tarda 64 0.047
325
NRN004 Neuroendocrine Tumor 56 0.047
326
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.047
327
CLC001 Calciphylaxis 46 0.047
328
GRM001 Germ Cell and Embryonal Cancer 36 0.047
329
c SYS001 Systemic Lupus Erythematosus 86 0.047
330
PRP030 Purpura 58 0.047
331
CTS003 Coats Disease 57 0.047
332
ERY003 Erythema Multiforme 55 0.047
333
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 50 0.047
334
DCB001 Decubitus Ulcer 41 0.047
335
c DRM035 Dermatitis, Atopic 2 36 0.047
336
P ALP009 Alopecia Areata 62 0.046
337
OCL009 Ocular Cancer 59 0.046
338
P NLD001 Nail Disease 54 0.046
339
P EPD003 Epidermolysis Bullosa Simplex 53 0.046
340
P CTN003 Cutaneous Lupus Erythematosus 48 0.046
341
MLL001 Molluscum Contagiosum 42 0.046
342
ALR002 Al-Raqad Syndrome 36 0.046
343
LGD001 Leg Dermatosis 16 0.046
344
P CLR023 Colorectal Cancer 97 0.045
345
P OBS005 Obesity 92 0.045
346
P PNM007 Pneumonia 68 0.045
347
DSC009 Discoid Lupus Erythematosus 45 0.045
348
BRS090 Breast Reconstruction 38 0.045
349
PHT003 Phototoxic Dermatitis 35 0.045
350
ABL002 Ablepharon-Macrostomia Syndrome 57 0.044
351
c CLL013 Cell Type Cancer 46 0.044
352
GRN007 Granuloma Annulare 37 0.044
353
ULC005 Ulcer of Lower Limbs 20 0.044
354
P ADN016 Adenocarcinoma 69 0.044
355
FCL009 Focal Dermal Hypoplasia 54 0.044
356
KDS001 Kid Syndrome 53 0.044
357
P SYP003 Syphilis 53 0.044
358
ERY021 Erythrokeratodermia Variabilis Et Progressiva 47 0.044
359
PMP004 Pemphigus Foliaceus 42 0.044
360
NRN002 Neuronitis 41 0.044
361
ALL003 Allergic Rhinitis 63 0.043
362
P HYP040 Hypospadias 57 0.043
363
P PRK001 Porokeratosis 45 0.043
364
ECT005 Ectropion 39 0.043
365
P DYS007 Dyskeratosis Congenita 63 0.042
366
P XRD010 Xeroderma Pigmentosum, Variant Type 58 0.042
367
c PSR017 Psoriasis 2 37 0.042
368
P SYR003 Syringoma 37 0.042
369
c ICH023 Ichthyosis, Acquired 19 0.042
370
P TBR001 Tuberous Sclerosis 67 0.041
371
ACN002 Acanthosis Nigricans 57 0.041
372
DBT010 Diabetic Neuropathy 55 0.041
373
PRT011 Protein C Deficiency 52 0.041
374
ERY017 Erythema Elevatum Diutinum 49 0.041
375
DRM011 Dermatophytosis 46 0.041
376
P ICH001 Ichthyosis Vulgaris 46 0.041
377
MYC019 Mycobacterium Marinum 28 0.041
378
c ATP016 Atopic Dermatitis 3 23 0.041
379
P PRP029 Porphyria 59 0.041
380
CHL071 Child Syndrome 58 0.041
381
P OCL002 Oculocutaneous Albinism 54 0.041
382
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.041
383
FLL008 Folliculitis 46 0.041
384
HDR003 Hidradenitis 45 0.041
385
P RHM011 Rheumatoid Arthritis 89 0.040
386
PCK002 Pick Disease 68 0.040
387
VSC007 Vascular Disease 67 0.040
388
P SML001 Small Cell Carcinoma 56 0.040
389
P CDS001 Cadasil 55 0.040
390
VND001 Vein Disease 47 0.040
391
ACR041 Acromelic Frontonasal Dysostosis 45 0.040
392
BRT030 Birth Defects 43 0.040
393
c RNL016 Renal Infectious Disease 20 0.040
394
c ATP017 Atopic Dermatitis 4 16 0.040
395
P ANP001 Anaplastic Large Cell Lymphoma 57 0.039
396
HLY001 Hailey-Hailey Disease 53 0.039
397
P EPD002 Epidermolytic Hyperkeratosis 50 0.039
398
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.039
399
LYM052 Lymphomatoid Papulosis 41 0.039
400
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.039
401
BLL012 Bullous Impetigo 35 0.039
402
GLB003 Globe Disease 32 0.039
403
c LCL022 Localized Lipodystrophy 30 0.039
404
RDT005 Radiation Induced Cancer 28 0.039
405
c ATP018 Atopic Dermatitis 5 15 0.039
406
c ST1001 St14-Related Autosomal Recessive Congenital Ichthyosis 10 0.039
407
c LPN003 Lipn-Related Autosomal Recessive Congenital Ichthyosis 10 0.039
408
c CYP003 Cyp4f22-Related Autosomal Recessive Congenital Ichthyosis 7 0.039
409
c ALX004 Alox12b-Related Autosomal Recessive Congenital Ichthyosis 7 0.039
410
c ALX005 Aloxe3-Related Autosomal Recessive Congenital Ichthyosis 7 0.039
411
c ABC002 Abca12-Related Autosomal Recessive Congenital Ichthyosis 7 0.039
412
c PNP002 Pnpla1-Related Autosomal Recessive Congenital Ichthyosis 7 0.039
413
c TGM001 Tgm1-Related Autosomal Recessive Congenital Ichthyosis 7 0.039
414
PRP027 Peripheral Vascular Disease 69 0.038
415
P INF037 Inflammatory Bowel Disease 63 0.038
416
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.038
417
P HST010 Histiocytosis 58 0.038
418
MCS002 Mucositis 55 0.038
419
P LCH002 Lichen Planus 53 0.038
420
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.038
421
URT001 Urethritis 41 0.038
422
SCL022 Scleredema 32 0.038
423
BRS051 Breast Disease 61 0.037
424
c ADL017 Adult T-Cell Leukemia 60 0.037
425
HRP004 Herpes Zoster 56 0.037
426
PRS047 Prostatitis 56 0.037
427
CMP010 Complex Regional Pain Syndrome 54 0.037
428
SML033 Small Cell Cancer of the Lung, Somatic 54 0.037
429
P VNS003 Venous Insufficiency 54 0.037
430
ADL002 Adult Syndrome 52 0.037
431
VCC001 Vaccinia 46 0.037
432
HYP077 Hypertrichosis 44 0.037
433
TNP001 Tinea Pedis 40 0.037
434
ICH031 Ichthyosis with Confetti 31 0.037
435
c BSL026 Basal Cell Carcinoma 3 16 0.037
436
P NRF002 Neurofibromatosis 71 0.037
437
ISC004 Ischemia 61 0.037
438
P MRT001 Muir-Torre Syndrome 59 0.037
439
P RTH001 Rothmund-Thomson Syndrome 55 0.037
440
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.037
441
PRT014 Protein S Deficiency 53 0.037
442
PNN001 Panniculitis 51 0.037
443
LPR001 Lepromatous Leprosy 50 0.037
444
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 48 0.037
445
PTY003 Pityriasis Rubra Pilaris 46 0.037
446
ALB002 Albinism 46 0.037
447
YWS001 Yaws 42 0.037
448
PTY001 Pityriasis Rosea 42 0.037
449
P PRP034 Purpura Fulminans 41 0.037
450
NCR002 Necrobiosis Lipoidica 32 0.037
451
HND001 Hand Dermatosis 23 0.037
452
P AMY004 Amyloidosis 65 0.036
453
MTH009 Mouth Disease 61 0.036
454
LYM024 Lymphatic System Disease 52 0.036
455
c CHR417 Chronic Graft Versus Host Disease 51 0.036
456
P HRD018 Hair Disease 51 0.036
457
URB001 Urbach-Wiethe Disease 49 0.036
458
P TCL004 T-Cell Leukemia 47 0.036
459
EPD028 Epidermolysis Bullosa Simplex, Dowling-Meara Type 45 0.036
460
PLL012 Pollen Allergy 44 0.036
461
EPD062 Epidermolysis Bullosa, Junctional, Non-Herlitz Type 44 0.036
462
DFF003 Diffuse Scleroderma 41 0.036
463
TRC010 Trichotillomania 40 0.036
464
BLD054 Blood Protein Disease 37 0.036
465
URT008 Urticaria Pigmentosa 37 0.036
466
SBC017 Sebaceous Gland Disease 34 0.036
467
c ICH040 Ichthyosis, Congenital, Autosomal Recessive 4a 29 0.036
468
c ICH038 Ichthyosis, Congenital, Autosomal Recessive 3 27 0.036
469
c ICH050 Ichthyosis, Congenital, Autosomal Recessive 5 26 0.036
470
ACR034 Acrogeria, Gottron Type 25 0.036
471
c ICH042 Ichthyosis, Congenital, Autosomal Recessive 6 25 0.036
472
c ICH044 Ichthyosis, Congenital, Autosomal Recessive 8 23 0.036
473
c ICH039 Ichthyosis, Congenital, Autosomal Recessive 10 22 0.036
474
c ICH048 Ichthyosis, Congenital, Autosomal Recessive 9 22 0.036
475
CST001 Costello Syndrome 68 0.035
476
HTC002 Hutchinson-Gilford Progeria 57 0.035
477
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.035
478
VRR004 Verrucous Carcinoma 54 0.035
479
P LTR001 Lateral Sclerosis 53 0.035
480
SZR001 Sezary's Disease 52 0.035
481
HYP542 Hypersensitivity Syndrome, Carbamazepine-Induced 52 0.035
482
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.035
483
NSD001 Nose Disease 48 0.035
484
HDN002 Head Injury 45 0.035
485
c EHL054 Ehlers-Danlos Syndrome, Type Vi 45 0.035
486
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.035
487
ERY004 Erysipelas 41 0.035
488
ANH002 Anhidrosis 41 0.035
489
PRL019 Prolidase Deficiency 38 0.035
490
ACR005 Acrodermatitis 36 0.035
491
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.035
492
c CTS019 Cutis Laxa, Ad 31 0.035
493
ADR007 Adrenoleukodystrophy 72 0.034
494
c HPT001 Hepatitis C 68 0.034
495
P MYP004 Myopathy 67 0.034
496
LYM115 Lymphoma, Non-Hodgkin 63 0.034
497
P CRD013 Cardiofaciocutaneous Syndrome 63 0.034
498
PBL001 Piebaldism 57 0.034
499
ORL011 Oral Cancer 56 0.034
500
P LYM033 Lymphoproliferative Syndrome 56 0.034
501
c EHL033 Ehlers-Danlos Syndrome, Classic Type 55 0.034
502
P ACT135 Acute Graft Versus Host Disease 53 0.034
503
CLN019 Colonic Disease 51 0.034
504
P CLL015 Collagen Disease 50 0.034
505
BSC001 Buschke-Ollendorff Syndrome 50 0.034
506
ONC002 Onchocerciasis 49 0.034
507
HST009 Histiocytoma 47 0.034
508
PRP082 Porphyria, Congenital Erythropoietic 46 0.034
509
CHR031 Chromoblastomycosis 42 0.034
510
c SCN006 Secondary Syphilis 41 0.034
511
PRP005 Parapsoriasis 39 0.034
512
c ICH041 Ichthyosis, Autosomal Recessive 4b 38 0.034
513
EPD061 Epidermolysis Bullosa, Junctional, Herlitz Type 38 0.034
514
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 36 0.034
515
EPD022 Epidermolysis Bullosa Pruriginosa 36 0.034
516
URT037 Urethral Stricture 33 0.034
517
CTS011 Cutis Marmorata Telangiectatica Congenita 30 0.034
518
HYP213 Hypomelanotic Disorder 21 0.034
519
BSL036 Basal Cell Nevus Syndrome 65 0.033
520
P LYM025 Lymphedema 61 0.033
521
c SRC025 Sarcoidosis 1 61 0.033
522
ALL006 Allergic Asthma 58 0.033
523
NRM005 Neuromuscular Disease 56 0.033
524
P EPD009 Epidermolysis Bullosa Dystrophica 55 0.033
525
RCT018 Rectal Neoplasm 54 0.033
526
FDL002 Food Allergy 53 0.033
527
ANG020 Angiosarcoma 53 0.033
528
LYM019 Lymphosarcoma 53 0.033
529
P SPS003 Spastic Diplegia 52 0.033
530
VSC006 Vascular Cancer 51 0.033
531
NPH018 Nephrogenic Systemic Fibrosis 51 0.033
532
c EHL055 Ehlers-Danlos Syndrome, Type Iii 50 0.033
533
P JNC001 Junctional Epidermolysis Bullosa 49 0.033
534
ACR003 Acrodermatitis Enteropathica 49 0.033
535
c ALB021 Albinism, Oculocutaneous, Type Ii 47 0.033
536
INC022 Inclusion-Cell Disease 46 0.033
537
PHY002 Physical Disorder 43 0.033
538
FBR003 Fibrous Histiocytoma 43 0.033
539
c ADL001 Adult Lymphoma 39 0.033
540
TNC003 Tinea Corporis 38 0.033
541
ART006 Arthus Reaction 37 0.033
542
MLD003 Meleda Disease 36 0.033
543
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 33 0.033
544
MLR009 Miliaria 32 0.033
545
c TRC078 Trichohepatoenteric Syndrome 2 29 0.033
546
MLR001 Miliaria Rubra 29 0.033
547
c SCL052 Scleroderma, Familial Progressive 27 0.033
548
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.033
549
c ICH045 Ichthyosis, Congenital, Autosomal Recessive 7 20 0.033
550
ERY010 Erythrasma 19 0.033
551
c BSL028 Basal Cell Carcinoma 5 16 0.033
552
c BCT003 Bacterial Exanthem 11 0.033
553
P RNL014 Renal Cell Carcinoma 82 0.032
554
P NRV007 Nervous System Disease 71 0.032
555
WRN001 Werner Syndrome 67 0.032
556
P CCK001 Cockayne Syndrome 61 0.032
557
MNK001 Menkes Disease 60 0.032
558
DRR010 Darier Disease 60 0.032
559
c SYS004 Systemic Mastocytosis 60 0.032
560
P GST049 Gastrointestinal System Cancer 60 0.032
561
BLS001 Blau Syndrome 57 0.032
562
CCT002 Cicatricial Pemphigoid 50 0.032
563
c XRD015 Xeroderma Pigmentosum, Group F 49 0.032
564
INT253 Intestinal Benign Neoplasm 47 0.032
565
c PSR021 Psoriasis 14, Pustular 46 0.032
566
c CHR431 Chronic Venous Insufficiency 44 0.032
567
PYG006 Pyogenic Granuloma 41 0.032
568
LCH009 Lichen Sclerosus 41 0.032
569
ADN002 Adenoiditis 39 0.032
570
CRB009 Cerebritis 39 0.032
571
LCH011 Lichen Planopilaris 39 0.032
572
CHR415 Chronic Venous Leg Ulcers 37 0.032
573
PRS063 Paresthesia 36 0.032
574
RDN001 Reading Disorder 34 0.032
575
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.032
576
SCR033 Scar Contracture 27 0.032
577
c BSL011 Basal Cell Carcinoma, Multiple 25 0.032
578
c CTS031 Cutis Laxa, Autosomal Dominant 2 22 0.032
579
ELS003 Elastoderma 14 0.032
580
P MLT019 Multiple Myeloma 83 0.031
581
FBR012 Fabry Disease 69 0.031
582
P MSC005 Muscular Dystrophy 65 0.031
583
LYM017 Lyme Disease 63 0.031
584
ACQ007 Acquired Immunodeficiency Syndrome 60 0.031
585
RHM027 Rheumatic Disease 58 0.031
586
ZLL001 Zellweger Syndrome 56 0.031
587
PRP019 Peripheral Nervous System Disease 55 0.031
588
P MCR129 Microvascular Complications of Diabetes 1 54 0.031
589
CHC001 Chickenpox 51 0.031
590
LPD004 Lipoid Nephrosis 48 0.031
591
RFL001 Reflex Sympathetic Dystrophy 48 0.031
592
CLR065 Colorectal Adenomatous Polyposis, Autosomal Recessive, with Pilomatricomas 45 0.031
593
P PLL002 Pellagra 45 0.031
594
ALN001 Aland Island Eye Disease 45 0.031
595
GDS001 Good Syndrome 44 0.031
596
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.031
597
PLM029 Palmoplantar Keratosis 43 0.031
598
STT007 Steatocystoma Multiplex 42 0.031
599
INT221 Intravascular Large B-Cell Lymphoma 38 0.031
600
LPD014 Lipodermatosclerosis 37 0.031
601
ELP001 Elephantiasis 37 0.031
602
P DWL001 Dowling-Degos Disease 36 0.031
603
c EHL028 Ehlers-Danlos Syndrome, Type Viii 35 0.031
604
EPD056 Epidermolysis Bullosa Simplex-Mp 34 0.031
605
LYM023 Lymphatic System Cancer 33 0.031
606
ACR097 Acrodermatitis Chronica Atrophicans 27 0.031
607
FCL045 Focal Facial Dermal Dysplasia 3, Setleis Type 22 0.031
608
c CTS037 Cutis Laxa, Autosomal Recessive, Type Ib 20 0.031
609
HRD113 Hereditary Acrokeratotic Poikiloderma, Weary Type 13 0.031
610
OMN001 Omenn Syndrome 67 0.030
611
P KDN017 Kidney Cancer 65 0.030
612
P THR014 Thrombocytopenia 64 0.030
613
CHR063 Chronic Mucocutaneous Candidiasis 63 0.030
614
c TBR024 Tuberous Sclerosis-1 63 0.030
615
P ORL007 Oral Cavity Cancer 59 0.030
616
ORL015 Oral Squamous Cell Carcinoma 57 0.030
617
P RBL001 Rubella 57 0.030
618
PLS011 Plasmacytoma 56 0.030
619
HYP266 Hypoxia 56 0.030
620
VRL011 Viral Infectious Disease 55 0.030
621
P END033 Endocarditis 54 0.030
622
SPT005 Spotted Fever 53 0.030
623
CRS005 Crest Syndrome 51 0.030
624
P CHR345 Chronic Pain 50 0.030
625
CSY001 C Syndrome 50 0.030
626
RYN003 Reynolds Syndrome 49 0.030
627
BCT015 Bacteremia 48 0.030
628
ECZ002 Eczema Herpeticum 47 0.030
629
MLT016 Multicentric Reticulohistiocytosis 46 0.030
630
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.030
631
ICH054 Ichthyosis, X-Linked 46 0.030
632
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 43 0.030
633
c ALB009 Albinism, Oculocutaneous, Type Ia 42 0.030
634
HMT018 Hematopoietic Stem Cell Transplantation 41 0.030
635
RCT017 Rectal Disease 40 0.030
636
PST053 Postherpetic Neuralgia 40 0.030
637
ADJ001 Adjustment Disorder 38 0.030
638
HYL004 Hyaline Fibromatosis Syndrome 38 0.030
639
CLD014 Cole Disease 37 0.030
640
KKC001 Kikuchi Disease 35 0.030
641
MSC004 Muscle Tissue Disease 34 0.030
642
PLC008 Placenta Disease 33 0.030
643
ENT005 Entropion 30 0.030
644
SPN370 Spondylodysplastic Ehlers-Danlos Syndrome 29 0.030
645
c CLR079 Colorectal Cancer 2 29 0.030
646
c AST037 Asthma 1 29 0.030
647
MYC015 Mycobacterium Fortuitum 28 0.030
648
MLK004 Malakoplakia 28 0.030
649
SLR005 Solar Urticaria 27 0.030
650
ATM052 Autoimmune Disease 1 25 0.030
651
P OST012 Osteoarthritis 83 0.029
652
MRF001 Marfan Syndrome 73 0.029
653
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.029
654
ANX002 Anxiety Disorder 67 0.029
655
P KDN018 Kidney Disease 66 0.029
656
P HYP098 Hypereosinophilic Syndrome 63 0.029
657
P HRM001 Hermansky-Pudlak Syndrome 59 0.029
658
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 59 0.029
659
ADN018 Adenoma 58 0.029
660
LYM021 Lymphadenitis 58 0.029
661
P FCS002 Fucosidosis 57 0.029
662
TLN003 Telangiectasis 52 0.029
663
MND007 Mandibuloacral Dysplasia 49 0.029
664
YLL001 Yellow Nail Syndrome 48 0.029
665
LMT001 Limited Scleroderma 46 0.029
666
ECT078 Ectodermal Dysplasia 2, Clouston Type 45 0.029
667
PRG004 Progeria 44 0.029
668
DBT008 Diabetic Angiopathy 44 0.029
669
EPD047 Epidermolysis Bullosa Simplex, Koebner Type 42 0.029
670
CHL028 Childhood Type Dermatomyositis 42 0.029
671
PRN049 Paraneoplastic Pemphigus 40 0.029
672
BND014 Bone Development Disease 40 0.029
673
SBC012 Subcorneal Pustular Dermatosis 40 0.029
674
c CCK006 Cockayne Syndrome, Type B 37 0.029
675
FXF002 Fox-Fordyce Disease 36 0.029
676
PRR013 Prurigo Nodularis 35 0.029
677
SPR005 Superficial Basal Cell Carcinoma 34 0.029
678
IMP003 Impaired Renal Function Disease 34 0.029
679
BWN006 Bowen's Disease 33 0.029
680
CHR463 Chronic Actinic Dermatitis 31 0.029
681
c ICH051 Ichthyosis, Congenital, Autosomal Recessive 11 30 0.029
682
HRZ001 Huriez Syndrome 30 0.029
683
PMP009 Pemphigus Erythematosus 30 0.029
684
CYL004 Cylindromatosis, Familial 29 0.029
685
OCL034 Oculocerebrocutaneous Syndrome 27 0.029
686
INF057 Inflammatory Linear Verrucous Epidermal Nevus 23 0.029
687
EPD031 Epidermolysis Bullosa Simplex, Ogna Type 22 0.029
688
SCL001 Scalp Dermatosis 18 0.029
689
c ATP019 Atopic Dermatitis 6 14 0.029
690
P PRS040 Prostate Cancer 90 0.028
691
P ATX030 Ataxia-Telangiectasia 77 0.028
692
c CHR090 Chronic Lymphocytic Leukemia 76 0.028
693
c HPT073 Hepatitis C Virus 73 0.028
694
P ALP004 Alport Syndrome 69 0.028
695
SVR004 Severe Combined Immunodeficiency 69 0.028
696
P OST005 Osteogenesis Imperfecta 69 0.028
697
SMT004 Smith-Lemli-Opitz Syndrome 66 0.028
698
P NMN002 Niemann-Pick Disease 65 0.028
699
P ART023 Arthropathy 64 0.028
700
BRN024 Bronchitis 64 0.028
701
MCK007 Muckle-Wells Syndrome 61 0.028
702
P SNS014 Sinusitis 60 0.028
703
P HYP035 Hypophosphatasia 57 0.028
704
SML019 Smallpox 54 0.028
705
P FML012 Familial Partial Lipodystrophy 52 0.028
706
P ANG015 Angioedema 52 0.028
707
OCL022 Ocular Melanoma 52 0.028
708
MVM001 Movement Disease 49 0.028
709
HYP074 Hypersensitivity Vasculitis 48 0.028
710
PST062 Pustulosis Palmaris Et Plantaris 48 0.028
711
FSC004 Fasciitis 48 0.028
712
GYN001 Gynecomastia 48 0.028
713
ANT024 Anthrax Disease 47 0.028
714
HND002 Hand, Foot and Mouth Disease 47 0.028
715
PRP021 Peripheral Nervous System Neoplasm 46 0.028
716
P HYP087 Hypotrichosis 46 0.028
717
CRY004 Cryoglobulinemia 46 0.028
718
PRP036 Peripheral T-Cell Lymphoma 45 0.028
719
ATN004 Autonomic Neuropathy 45 0.028
720
CRN024 Corneal Disease 44 0.028
721
DFF001 Diffuse Cutaneous Mastocytosis 43 0.028
722
VHW001 Vohwinkel Syndrome 41 0.028
723
c CCK005 Cockayne Syndrome, Type a 39 0.028
724
MLG088 Malignant Germ Cell Tumor 38 0.028
725
WTH001 Withdrawal Disorder 37 0.028
726
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.028
727
ATM012 Autoimmune Disease of Blood 35 0.028
728
PMP002 Pemphigoid Gestationis 35 0.028
729
OCC001 Occupational Dermatitis 34 0.028
730
ACR002 Acrocapitofemoral Dysplasia 33 0.028
731
c EHL027 Ehlers-Danlos Syndrome, Type Viic 32 0.028
732
LCH013 Lichen Planus Pemphigoides 32 0.028
733
ALL007 Allergic Urticaria 31 0.028
734
PLM135 Palmoplantar Keratoderma, Bothnian Type 30 0.028
735
ERY001 Erysipeloid 30 0.028
736
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 30 0.028
737
ATY016 Atypical Werner Syndrome 28 0.028
738
P PHT010 Photoparoxysmal Response 1 28 0.028
739
c KRT055 Keratoderma, Palmoplantar, Punctate Type Ia 26 0.028
740
TRN023 Transient Bullous of the Newborn 24 0.028
741
c EFM001 Efemp2-Related Cutis Laxa 18 0.028
742
c FBL003 Fbln5-Related Cutis Laxa 16 0.028
743
c ALD008 Aldh18a1-Related Cutis Laxa 16 0.028
744
c BSL029 Basal Cell Carcinoma 6 16 0.028
745
c BSL027 Basal Cell Carcinoma 4 15 0.028
746
c ATP020 Atopic Dermatitis 7 15 0.028
747
c ATP021 Atopic Dermatitis 8 14 0.028
748
c LTB003 Ltbp4-Related Cutis Laxa 14 0.028
749
c PYC002 Pycr1-Related Cutis Laxa 12 0.028
750
c ELN002 Eln-Related Cutis Laxa 8 0.028
751
P HPT023 Hepatocellular Carcinoma 92 0.026
752
P PNC035 Pancreatic Cancer 87 0.026
753
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.026
754
P HRT032 Heart Disease 75 0.026
755
P PLM036 Pulmonary Fibrosis 71 0.026
756
PLM001 Pulmonary Tuberculosis 67 0.026
757
c NRF018 Neurofibromatosis, Type 1 67 0.026
758
P THN009 Thanatophoric Dysplasia, Type I 63 0.026
759
P RCK004 Rickets 61 0.026
760
P MCP010 Mucopolysaccharidosis 60 0.026
761
WLL001 Williams-Beuren Syndrome 60 0.026
762
CRV038 Cervical Squamous Cell Carcinoma 60 0.026
763
P PNL012 Penile Cancer 58 0.026
764
SFT003 Soft Tissue Sarcoma 57 0.026
765
RBS003 Rabson-Mendenhall Syndrome 55 0.026
766
END030 End Stage Renal Failure 55 0.026
767
SLP005 Sleep Disorder 53 0.026
768
c INS002 in Situ Carcinoma 53 0.026
769
P ATX004 Ataxia 53 0.026
770
FML037 Female Breast Cancer 50 0.026
771
PRP032 Porphyria Variegata 50 0.026
772
CHL069 Cholesteatoma 49 0.026
773
PPL049 Papillon-Lefevre Syndrome 48 0.026
774
LYM051 Lymphomatoid Granulomatosis 47 0.026
775
EPD045 Epidermolysis Bullosa, Junctional, with Pyloric Stenosis 46 0.026
776
HPR003 Heparin-Induced Thrombocytopenia 45 0.026
777
P CRV039 Cervicitis 45 0.026
778
VSC047 Vascular Malformation 45 0.026
779
ACD009 Acid-Labile Subunit, Deficiency of 45 0.026
780
TBR006 Tuberculoid Leprosy 43 0.026
781
BCK006 Back Pain 43 0.026
782
c EHL018 Ehlers-Danlos Syndrome Type Ii 42 0.026
783
MYC013 Mycobacterium Abscessus 41 0.026
784
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.026
785
HMN016 Hemangioendothelioma 39 0.026
786
MCR103 Microtia 37 0.026
787
ANG037 Angiomatosis 37 0.026
788
P PST059 Pustular Psoriasis 36 0.026
789
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.026
790
ADN013 Adenoid Squamous Cell Carcinoma 36 0.026
791
LNT002 Lentigo Maligna Melanoma 35 0.026
792
NVS007 Nevus of Ota 34 0.026
793
SWT003 Sweat Gland Disease 34 0.026
794
OCH001 Ochronosis 33 0.026
795
PRK010 Porokeratosis of Mibelli 33 0.026
796
SCL025 Scleromyxedema 32 0.026
797
MYC014 Mycobacterium Chelonae 32 0.026
798
TNC001 Tinea Cruris 31 0.026
799
KRT044 Keratosis Pilaris 30 0.026
800
c ALB010 Albinism, Oculocutaneous, Type Ib 30 0.026
801
EPD040 Epidermolysis Bullosa Simplex with Pyloric Atresia 30 0.026
802
c AST039 Asthma 2 28 0.026
803
c CTS008 Cutis Laxa, Autosomal Dominant 28 0.026
804
P MLT048 Multiple Familial Trichoepithelioma 28 0.026
805
GRD005 Geroderma Osteodysplasticum 26 0.026
806
CCT001 Cicatricial Ectropion 25 0.026
807
FLL019 Follicular Mucinosis 25 0.026
808
HYP160 Hyperkeratosis Lenticularis Perstans 23 0.026
809
PSD078 Pseudofolliculitis Barbae 21 0.026
810
c KRT056 Keratosis Palmoplantaris Striata I, Ad 20 0.026
811
FCL067 Focal Facial Dermal Dysplasia 1, Brauer Type 19 0.026
812
PGM028 Pigmented Purpuric Dermatosis 18 0.026
813
c PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 18 0.026
814
ATM053 Autoimmune Disease 2 16 0.026
815
LNR009 Linear Atrophoderma of Moulin 14 0.026
816
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.025
817
P LVR013 Liver Disease 75 0.025
818
GST019 Gastrointestinal Stromal Tumor 73 0.025
819
KWS002 Kawasaki Disease 70 0.025
820
BRC012 Brucellosis 66 0.025
821
CHR012 Chronic Granulomatous Disease 65 0.025
822
MSL001 Measles 61 0.025
823
BHC003 Behcet Syndrome 60 0.025
824
ADL030 Adult-Onset Still's Disease 59 0.025
825
P SHR029 Short Syndrome 58 0.025
826
P MCR010 Microcephaly 58 0.025
827
c XRD018 Xeroderma Pigmentosum, Group a 57 0.025
828
BTN003 Biotinidase Deficiency 57 0.025
829
ETH011 Ethylmalonic Encephalopathy 56 0.025
830
JNT002 Joint Disorders 55 0.025
831
CCC001 Coccidioidomycosis 55 0.025
832
P LMY004 Leiomyosarcoma 55 0.025
833
CPR001 Coproporphyria 53 0.025
834
ERD001 Erdheim-Chester Disease 52 0.025
835
c XRD019 Xeroderma Pigmentosum, Group C 52 0.025
836
P MSC033 Muscle Disorders 52 0.025
837
HST011 Histoplasmosis 52 0.025
838
P ERY008 Erythromelalgia 51 0.025
839
ART001 Arterial Tortuosity Syndrome 50 0.025
840
LRN003 Learning Disability 49 0.025
841
P INT063 Intellectual Disability 49 0.025
842
LMB062 Limb Ischemia 48 0.025
843
ATN002 Autonomic Nervous System Disease 48 0.025
844
P GRN010 Granular Cell Tumor 47 0.025
845
PRN014 Paronychia 47 0.025
846
GLC036 Glucagonoma 46 0.025
847
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 45 0.025
848
KRT036 Keratosis, Seborrheic, Somatic 45 0.025
849
c CLR085 Colorectal Cancer 1 45 0.025
850
FBR019 Fibromatosis 43 0.025
851
LKC003 Leukocyte Disease 43 0.025
852
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.025
853
WRD025 Waardenburg Syndrome, Type 2e, with or Without Neurologic Involvement 42 0.025
854
SXL003 Sexual Disorder 42 0.025
855
HYP458 Hyper Ige Syndrome 42 0.025
856
FCT008 Factitious Disorder 41 0.025
857
P BRT029 Brittle Cornea Syndrome 2 41 0.025
858
MLN013 Melanoma Metastasis 40 0.025
859
PNC085 Penicillin Allergy 40 0.025
860
MNN021 Meningococcemia 39 0.025
861
NRC019 Neurocutaneous Melanosis, Somatic 39 0.025
862
c CLL012 Cell Type Benign Neoplasm 39 0.025
863
HYP022 Hypohidrosis 37 0.025
864
EPD065 Epidermolytic Ichthyosis 37 0.025
865
DRC001 Dracunculiasis 37 0.025
866
BZX001 Bazex Syndrome 35 0.025
867
ECT004 Ecthyma 35 0.025
868
CRC001 Cercarial Dermatitis 35 0.025
869
HRP002 Herpes Gestationis 34 0.025
870
MJD001 Majeed Syndrome 33 0.025
871
c CNN010 Connective Tissue Benign Neoplasm 32 0.025
872
BRD005 Borderline Leprosy 32 0.025
873
DRM003 Dermatosis Papulosa Nigra 32 0.025
874
GTT002 Guttate Psoriasis 31 0.025
875
c MLN032 Melanoma, Cutaneous Malignant, 2 31 0.025
876
ACN010 Acanthoma 31 0.025
877
ELS002 Elastosis Perforans Serpiginosa 30 0.025
878
EHL060 Ehlers-Danlos Syndrome Due to Tenascin X Deficiency 29 0.025
879
c CTS038 Cutis Laxa, Autosomal Recessive, Type Iia 25 0.025
880
LPS019 Lupus Erythematosus Tumidus 21 0.025
881
GNT018 Gianotti Crosti Syndrome 21 0.025
882
EPD057 Epidermylysis Bullosa Simplex-Mcr 21 0.025
883
ERS002 Erosive Pustular Dermatosis of the Scalp 20 0.025
884
c EHL065 Ehlers-Danlos Syndrome, Type V 18 0.025
885
EPD052 Epidermolysis Bullosa Simplex Superficialis 18 0.025
886
c DRM040 Dermatitis Herpetiformis, Familial 17 0.025
887
CTN032 Cutaneous Mastocytosis, Conductive Hearing Loss and Microtia 14 0.025
888
c RTH004 Rothmund-Thomson Syndrome Type 1 14 0.025
889
P LNG032 Lung Cancer 95 0.024
890
INS024 Insulin-Like Growth Factor I 75 0.024
891
P WSK001 Wiskott-Aldrich Syndrome 73 0.024
892
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.024
893
P MTC003 Metachromatic Leukodystrophy 70 0.024
894
P CSH001 Cushing's Syndrome 65 0.024
895
AND015 Androgen Insensitivity 64 0.024
896
P CNJ013 Conjunctivitis 64 0.024
897
PRT036 Peritonitis 63 0.024
898
P ADD001 Addison's Disease 62 0.024
899
TNG002 Tangier Disease 62 0.024
900
P PNC044 Pancreatitis 61 0.024
901
EYD002 Eye Disease 61 0.024
902
P TMP003 Temporal Arteritis 60 0.024
903
PRM097 Primary Immunodeficiency Disease 60 0.024
904
c VRL010 Viral Hepatitis 60 0.024
905
LPM004 Lipoma 60 0.024
906
P DRR001 Diarrhea 60 0.024
907
SPT004 Septic Arthritis 60 0.024
908
P NTR004 Neutropenia 59 0.024
909
P LKD001 Leukodystrophy 59 0.024
910
P UVT001 Uveitis 58 0.024
911
ALP001 Alopecia Universalis 58 0.024
912
P MSC007 Muscle Hypertrophy 58 0.024
913
BNC003 Bone Cancer 58 0.024
914
P CND004 Candidiasis 57 0.024
915
RHB003 Rhabdomyosarcoma 57 0.024
916
THR024 Thrombosis 57 0.024
917
PRT093 Proteus Syndrome, Somatic 56 0.024
918
P LPR002 Leopard Syndrome 55 0.024
919
PRC002 Paracoccidioidomycosis 55 0.024
920
P WRD001 Waardenburg's Syndrome 55 0.024
921
P MNC007 Monocytic Leukemia 55 0.024
922
P LRY019 Laryngitis 54 0.024
923
PTT049 Pituitary Adenoma, Acth-Secreting 53 0.024
924
NRF007 Neurofibroma 53 0.024
925
DSS008 Disease of Mental Health 52 0.024
926
PRT058 Pure Autonomic Failure 52 0.024
927
RTN023 Retinitis 50 0.024
928
MST017 Mast Cell Disease 50 0.024
929
P PRM001 Primary Cutaneous Amyloidosis 50 0.024
930
P PCH015 Pachyonychia Congenita 1 49 0.024
931
MCR088 Microscopic Polyangiitis 49 0.024
932
CTN014 Cutaneous Mastocytosis 49 0.024
933
NNN026 Noonan Syndrome with Multiple Lentigines 48 0.024
934
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 47 0.024
935
SPH001 Sapho Syndrome 46 0.024
936
SCR002 Scurvy 46 0.024
937
FBR054 Fibroma 46 0.024
938
HRT031 Hartnup Disorder 45 0.024
939
SND002 Sneddon Syndrome 44 0.024
940
P INF049 Infantile Myofibromatosis 43 0.024
941
GLC008 Glucose Metabolism Disease 42 0.024
942
RPR002 Reproductive System Disease 41 0.024
943
EGG001 Egg Allergy 41 0.024
944
TTR011 Tetraploidy 41 0.024
945
P CNN004 Connective Tissue Cancer 40 0.024
946
FML091 Familial Tumoral Calcinosis 39 0.024
947
CMM003 Common Wart 39 0.024
948
BDY001 Body Dysmorphic Disorder 39 0.024
949
SWT002 Sweat Gland Cancer 39 0.024
950
SPC003 Specific Developmental Disorder 38 0.024
951
TNG001 Tungiasis 37 0.024
952
NTR005 Nutritional Deficiency Disease 36 0.024
953
ADP001 Adiposis Dolorosa 36 0.024
954
LCH004 Lichen Disease 36 0.024
955
RTC008 Reticulate Acropigmentation of Kitamura 34 0.024
956
EPD033 Epidermolysis Bullosa, Lethal Acantholytic 34 0.024
957
PRL042 Proliferating Trichilemmal Cyst 33 0.024
958
CLD011 Cold Urticaria 33 0.024
959
c HYP373 Hyper-Ige Recurrent Infection Syndrome, Autosomal Recessive 33 0.024
960
c ALB019 Albinism, Oculocutaneous, Type Iv 32 0.024
961
LBM003 Lobomycosis 32 0.024
962
HYW001 Hay-Wells Syndrome 32 0.024
963
XRD026 Xeroderma Pigmentosum-Cockayne Syndrome Complex 32 0.024
964
TRT003 Tertiary Syphilis 31 0.024
965
DRM008 Dermatographia 31 0.024
966
P DMN011 Dominant Dystrophic Epidermolysis Bullosa 30 0.024
967
HNS001 Hansen's Disease 30 0.024
968
VSC008 Vascular Hemostatic Disease 30 0.024
969
c EHL041 Ehlers-Danlos Syndrome, Type Vii 29 0.024
970
VBR001 Vibratory Urticaria 29 0.024
971
c CTS023 Cutis Laxa, Autosomal Recessive, Type Iib 28 0.024
972
EPD034 Epidermolysis Bullosa, Pretibial 27 0.024
973
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 26 0.024
974
CNG133 Congenital Varicella Syndrome 26 0.024
975
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 26 0.024
976
NTR042 Neutrophilic Dermatosis, Acute Febrile 25 0.024
977
CRY006 Cryofibrinogenemia 25 0.024
978
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 24 0.024
979
SPN180 Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like 24 0.024
980
BCL011 Bacillary Angiomatosis 24 0.024
981
c EPD043 Epidermolysis Bullosa Dystrophica, Ad 20 0.024
982
P PRM145 Primary Anetoderma 20 0.024
983
P HYD015 Hydroa Vacciniforme 20 0.024
984
ARG004 Argyria 20 0.024
985
QNQ001 Quinquaud's Decalvans Folliculitis 19 0.024
986
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 17 0.024
987
c FCL046 Focal Facial Dermal Dysplasia 4 17 0.024
988
c DMN009 Dominant Ichthyosis Vulgaris 16 0.024
989
RMB001 Rombo Syndrome 16 0.024
990
AND005 Androgen Insensitivity Syndrome, Mild 16 0.024
991
CTN031 Cutaneous Pseudolymphoma 14 0.024
992
c ATS072 Autosomal Recessive Palmoplantar Keratoderma and Congenital Alopecia 14 0.024
993
c LPR019 Lipe-Related Familial Partial Lipodystrophy 13 0.024
994
PRK076 Porokeratosis 2, Palmar, Plantar, and Disseminated Type 13 0.024
995
c ATS003 Autosomal Recessive Type Iv Ehlers-Danlos Syndrome 8 0.024
996
ATR020 Atrophoderma of Pierini and Pasini 7 0.024
997
ULC004 Ulcerative Colitis 76 0.023
998
P LYN001 Lynch Syndrome 69 0.023
999
P MNN013 Meningitis 67 0.023
1000
ACR007 Acromegaly 66 0.023
1001
P TRN020 Turner Syndrome 65 0.023
1002
c HPT016 Hepatitis B 65 0.023
1003
P CWD001 Cowden Disease 64 0.023
1004
CHD001 Chediak-Higashi Syndrome 64 0.023
1005
LNG099 Lung Disease 64 0.023
1006
WGN006 Wegener Granulomatosis 63 0.023
1007
MXD005 Mixed Connective Tissue Disease 62 0.023
1008
APH001 Aphthous Stomatitis 62 0.023
1009
P PRD006 Prader-Willi Syndrome 62 0.023
1010
OST017 Osteomyelitis 61 0.023
1011
P ASP006 Aspergillosis 61 0.023
1012
c CNT035 Central Nervous System Disease 60 0.023
1013
SCH014 Schistosomiasis 58 0.023
1014
EMB004 Embryonal Carcinoma 57 0.023
1015
c CWD006 Cowden Syndrome 1 57 0.023
1016
P AGM005 Agammaglobulinemia, X-Linked 1 57 0.023
1017
P ANT006 Antiphospholipid Syndrome 56 0.023
1018
ART111 Artery Disease 55 0.023
1019
P LPD010 Lipodystrophy 55 0.023
1020
VGT001 Vogt-Koyanagi-Harada Disease 55 0.023
1021
OSS012 Osseous Heteroplasia, Progressive 54 0.023
1022
P LPC002 Lip Cancer 53 0.023
1023
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 53 0.023
1024
P SML016 Small Intestine Cancer 52 0.023
1025
BRT002 Birt-Hogg-Dube Syndrome 52 0.023
1026
CRT049 Critical Limb Ischemia 51 0.023
1027
c WRD030 Waardenburg Syndrome, Type 1 51 0.023
1028
MYL020 Myelomeningocele 51 0.023
1029
c GRS014 Griscelli Syndrome, Type 2 51 0.023
1030
INF034 Infective Endocarditis 51 0.023
1031
P PLY017 Polyarteritis Nodosa 51 0.023
1032
SCH002 Schnitzler Syndrome 51 0.023
1033
CLF001 Cleft Lip 50 0.023
1034
CLC006 Calcinosis 50 0.023
1035
P HMC002 Homocystinuria 50 0.023
1036
URN009 Urinary System Disease 50 0.023
1037
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.023
1038
P URF003 Urofacial Syndrome 1 50 0.023
1039
CHN055 Chanarin-Dorfman Syndrome 49 0.023
1040
MCP006 Mucoepidermoid Carcinoma 48 0.023
1041
P ADM011 Adams-Oliver Syndrome 48 0.023
1042
PPL046 Popliteal Pterygium Syndrome 1 47 0.023
1043
c TRC091 Trichorhinophalangeal Syndrome, Type Ii 47 0.023
1044
SPR010 Sporotrichosis 47 0.023
1045
VLV044 Vulvar Intraepithelial Neoplasia 47 0.023
1046
PRS039 Prostate Adenocarcinoma 46 0.023
1047
CTS002 Cat-Scratch Disease 46 0.023
1048
P TMR011 Tumoral Calcinosis, Hyperphosphatemic, Familial 46 0.023
1049
DYS022 Dyschromatosis Symmetrica Hereditaria 46 0.023
1050
P MRC003 Mercury Poisoning 45 0.023
1051
c ATS013 Autosomal Recessive Congenital Ichthyosis 45 0.023
1052
ICH002 Ichthyosis Bullosa of Siemens 45 0.023
1053
MXD023 Mixed Cell Type Cancer 45 0.023
1054
CHR008 Choroiditis 44 0.023
1055
PLS030 Plasminogen Deficiency, Type I 44 0.023
1056