Search results for Melanin

438 hits were found for Melanin

# Family MCID Name MIFTS Score
1
DSR014 Disorder of Melanin Metabolism 3 2.965
2
c DWL002 Dowling-Degos Disease 1 58 0.324
3
P MLN008 Melanoma 69 0.301
4
MCR013 Microphthalmia 57 0.299
5
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.246
6
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.222
7
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.222
8
P SKN015 Skin Carcinoma 66 0.210
9
PRT037 Pertussis 65 0.176
10
P UVT001 Uveitis 57 0.176
11
ALB002 Albinism 46 0.154
12
PST092 Posttransplant Acute Limbic Encephalitis 29 0.150
13
LNT004 Lentigines 50 0.140
15
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.128
16
IRD001 Iridocyclitis 53 0.120
17
SKN016 Skin Disease 63 0.111
18
P OCL002 Oculocutaneous Albinism 60 0.111
19
AML001 Amelanotic Melanoma 39 0.111
20
c ALB021 Albinism, Oculocutaneous, Type Ii 59 0.101
21
P NRC002 Narcolepsy 52 0.101
22
P NRB001 Neuroblastoma 72 0.096
23
PTZ001 Peutz-Jeghers Syndrome 70 0.096
24
THY111 Thyroid Carcinoma, Familial Medullary 67 0.096
25
THY029 Thyroid Carcinoma 59 0.096
26
THY125 Thyroid Gland Medullary Carcinoma 50 0.096
27
PPL052 Papillomatosis, Confluent and Reticulated 33 0.096
28
INT358 Intestinal Polyposis Syndrome 25 0.096
29
SKN019 Skin Melanoma 68 0.091
30
P RTN018 Retinal Disease 53 0.091
31
c CLR017 Clear Cell Sarcoma 45 0.091
32
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.091
33
P SLP005 Sleep Disorder 59 0.085
34
PGM030 Pigmentation Anomaly of the Skin 26 0.085
35
ANX010 Anxiety 73 0.079
36
P PHC003 Pheochromocytoma 71 0.079
37
SRC014 Sarcoma 65 0.079
38
CHL014 Cholera 59 0.079
39
SPN035 Spindle Cell Sarcoma 53 0.079
40
PGM003 Pigmentation Disease 46 0.079
42
MLN073 Melanosis, Neurocutaneous 45 0.079
43
P ASP006 Aspergillosis 69 0.072
44
ATM095 Autoimmune Disease 62 0.072
45
DBN001 Dubin-Johnson Syndrome 59 0.072
46
ADN018 Adenoma 59 0.072
47
CRY005 Cryptococcosis 58 0.072
48
c ALB009 Albinism, Oculocutaneous, Type Ia 57 0.072
49
AGN016 Aging 56 0.072
50
VGT001 Vogt-Koyanagi-Harada Disease 55 0.072
51
P INF037 Inflammatory Bowel Disease 54 0.072
52
OCL022 Ocular Melanoma 50 0.072
53
CHR031 Chromoblastomycosis 47 0.072
54
SPR010 Sporotrichosis 46 0.072
55
CHR008 Choroiditis 46 0.072
56
ADR040 Adrenal Gland Pheochromocytoma 46 0.072
57
TCH005 Tièche-Jadassohn Nevus 28 0.072
58
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 28 0.072
59
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.064
60
MDD011 Mood Disorder 62 0.064
61
FTT001 Fatty Liver Disease 61 0.064
62
DRM006 Dermatitis 61 0.064
63
RTN017 Retinal Detachment 61 0.064
64
P MLN069 Melanoma, Uveal 59 0.064
65
P NRF002 Neurofibromatosis 56 0.064
66
PRC002 Paracoccidioidomycosis 54 0.064
67
FNG017 Fungal Infectious Disease 53 0.064
68
INT051 Intussusception 53 0.064
69
P OCL001 Ocular Albinism 50 0.064
70
47X002 47,xyy 49 0.064
71
RTN023 Retinitis 46 0.064
72
c ATM099 Autoimmune Uveitis 45 0.064
73
PHH001 Phaeohyphomycosis 42 0.064
74
NRR001 Neuroretinitis 42 0.064
75
CLD014 Cole Disease 40 0.064
76
P TRC031 Trichorhinophalangeal Syndrome 40 0.064
77
48X005 48,xyyy 39 0.064
78
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.064
79
PLY150 Polykaryocytosis Inducer 31 0.064
80
CHL098 Childhood Myocerebrohepatopathy Spectrum 19 0.064
81
OST012 Osteoarthritis 78 0.056
82
P PRK057 Parkinson Disease, Late-Onset 78 0.056
83
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.056
84
DFC004 Deficiency Anemia 70 0.056
85
c BSL007 Basal Cell Carcinoma 68 0.056
86
P DRM053 Dermatitis, Atopic 66 0.056
87
P HRM001 Hermansky-Pudlak Syndrome 64 0.056
88
NRF007 Neurofibroma 64 0.056
89
INC021 Incontinentia Pigmenti 63 0.056
90
P GLM045 Glioma 63 0.056
91
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.056
92
DPH001 Diphtheria 60 0.056
93
IRN001 Iron Deficiency Anemia 59 0.056
94
ALK013 Alkaptonuria 58 0.056
95
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.056
96
IRN002 Iron Metabolism Disease 57 0.056
97
HYP060 Hyperinsulinism 54 0.056
98
P LCH002 Lichen Planus 53 0.056
99
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.056
100
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.056
101
MCP006 Mucoepidermoid Carcinoma 50 0.056
102
P OPN001 Open-Angle Glaucoma 49 0.056
103
VCC001 Vaccinia 49 0.056
104
P TRT019 Torticollis 48 0.056
105
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.056
106
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.056
107
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.056
108
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.056
109
GLL048 Glial Tumor 45 0.056
110
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.056
111
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.056
112
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.056
113
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.056
114
FBR054 Fibroma 44 0.056
115
ODN006 Odontoma 31 0.056
116
P FML313 Familial Progressive Hyperpigmentation 28 0.056
117
ARG004 Argyria 27 0.056
118
SPR033 Superficial Spreading Melanoma 18 0.056
119
P BRS047 Breast Cancer 97 0.045
120
P MDL005 Medulloblastoma 77 0.045
121
P SCH015 Schizophrenia 74 0.045
122
P RTN024 Retinoblastoma 73 0.045
123
P FLL037 Follicular Lymphoma 67 0.045
124
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.045
125
CHD001 Chediak-Higashi Syndrome 66 0.045
126
KRT019 Keratitis, Hereditary 65 0.045
127
TBC004 Tobacco Addiction 64 0.045
128
P PRD008 Periodontitis 64 0.045
129
DPR016 Depression 63 0.045
130
P PLY014 Polycystic Kidney Disease 62 0.045
131
c BRN108 Branchiootic Syndrome 1 62 0.045
132
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.045
133
NRL005 Neurilemmoma 60 0.045
134
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.045
135
ETN001 Eating Disorder 60 0.045
136
GNG013 Gingivitis 59 0.045
137
RBS001 Rabies 58 0.045
138
CNT047 Contact Dermatitis 58 0.045
139
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.045
140
EYD002 Eye Disease 58 0.045
141
P SLV026 Salivary Gland Carcinoma 57 0.045
142
P PRN023 Prion Disease 57 0.045
143
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.045
144
P NRP001 Neuropathy 56 0.045
145
P GST044 Gastritis 56 0.045
146
TRD006 Tardive Dyskinesia 54 0.045
147
c ALB010 Albinism, Oculocutaneous, Type Ib 54 0.045
148
P ALP008 Alopecia 54 0.045
149
P ICH004 Ichthyosis 54 0.045
150
HMS001 Hemosiderosis 54 0.045
151
P CNG010 Congenital Stationary Night Blindness 54 0.045
152
NNL006 Non-Alcoholic Steatohepatitis 54 0.045
153
MMM001 Mammary Paget's Disease 53 0.045
154
P RTN016 Retinal Degeneration 53 0.045
155
DNT012 Dental Caries 53 0.045
156
c FML008 Familial Retinoblastoma 53 0.045
157
PLM014 Pleomorphic Adenoma 52 0.045
158
P TRT010 Teratoma 52 0.045
159
c HRM005 Hermansky-Pudlak Syndrome 1 51 0.045
160
KRT009 Keratosis 51 0.045
161
CLR109 Colorectal Adenocarcinoma 51 0.045
162
ENT011 Enterocolitis 51 0.045
163
c GRS014 Griscelli Syndrome, Type 2 50 0.045
164
MYC012 Mycetoma 49 0.045
165
c INV001 Invasive Aspergillosis 49 0.045
166
ATS010 Autosomal Recessive Disease 48 0.045
167
GNG008 Ganglioneuroblastoma 48 0.045
168
SYM002 Sympathetic Ophthalmia 47 0.045
169
HLX001 Helix Syndrome 47 0.045
170
c HRM007 Hermansky-Pudlak Syndrome 4 46 0.045
171
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.045
172
c GRS013 Griscelli Syndrome, Type 1 44 0.045
173
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.045
174
OVR063 Overnutrition 44 0.045
175
CYT002 Cytokine Deficiency 42 0.045
176
P CYS017 Cystic Teratoma 41 0.045
177
P HYP263 Hypersomnia 41 0.045
178
P RRH023 Rare Hereditary Hemochromatosis 41 0.045
179
OCH001 Ochronosis 38 0.045
180
HYP744 Hyperpigmentation with or Without Hypopigmentation, Familial Progressive 38 0.045
181
HRN029 Hearing Loss, Noise-Induced 37 0.045
182
SPT007 Spitz Nevus 34 0.045
183
PGM029 Pigmentary Disorder, Reticulate, with Systemic Manifestations, X-Linked 34 0.045
184
ACR025 Acrocephalopolydactylous Dysplasia 33 0.045
185
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.045
186
MNG001 Mongolian Spot 31 0.045
187
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 31 0.045
188
c ALB017 Albinism, Oculocutaneous, Type Vi 30 0.045
189
NVS007 Nevus of Ota 28 0.045
190
NRL008 Neural Crest Tumor 27 0.045
191
STN013 Stenotrophomonas Maltophilia Infection 25 0.045
192
NVD003 Nevoid Hypermelanosis, Linear and Whorled 23 0.045
193
ACR040 Acromelanosis 12 0.045
194
P HPT023 Hepatocellular Carcinoma 100 0.032
195
P OVR042 Ovarian Cancer 88 0.032
196
P ALZ034 Alzheimer Disease 88 0.032
197
P ATX030 Ataxia-Telangiectasia 82 0.032
198
MLR004 Malaria 81 0.032
199
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.032
200
c NRF023 Neurofibromatosis, Type Ii 80 0.032
201
P RTN008 Retinitis Pigmentosa 79 0.032
202
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.032
203
c TBR025 Tuberous Sclerosis 1 77 0.032
204
PHN003 Phenylketonuria 75 0.032
205
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.032
206
VNH007 Von Hippel-Lindau Syndrome 73 0.032
207
c HYP836 Hypercholesterolemia, Familial, 1 73 0.032
208
P KDN018 Kidney Disease 72 0.032
209
P HNT016 Huntington Disease 72 0.032
210
OTT002 Otitis Media 72 0.032
211
c LKM063 Leukemia, Chronic Myeloid 72 0.032
212
HMN044 Human Immunodeficiency Virus Type 1 71 0.032
213
c EXD008 Exudative Vitreoretinopathy 1 71 0.032
214
P ATS364 Autism 70 0.032
215
P AMY004 Amyloidosis 70 0.032
216
ADN011 Adenoid Cystic Carcinoma 70 0.032
217
P MYP004 Myopathy 70 0.032
218
P TBR001 Tuberous Sclerosis 70 0.032
219
P OCL013 Oculodentodigital Dysplasia 69 0.032
220
P HYP086 Hypothyroidism 69 0.032
221
P LPR021 Leprosy 3 69 0.032
222
MST024 Mastocytosis, Cutaneous 69 0.032
223
P SYS005 Systemic Scleroderma 68 0.032
224
OBS002 Obsessive-Compulsive Disorder 68 0.032
225
RCK004 Rickets 68 0.032
226
P MJR001 Major Depressive Disorder 68 0.032
227
ALL003 Allergic Rhinitis 67 0.032
228
P CHR012 Chronic Granulomatous Disease 67 0.032
229
c ATS007 Autism Spectrum Disorder 67 0.032
230
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.032
231
HYP056 Hypoglycemia 66 0.032
232
CHG001 Chagas Disease 66 0.032
233
c SML038 Small Cell Cancer of the Lung 65 0.032
234
CRN036 Craniopharyngioma 65 0.032
235
DRM014 Dermatofibrosarcoma Protuberans 65 0.032
236
MNK001 Menkes Disease 64 0.032
237
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.032
238
P MST009 Mastocytosis 64 0.032
239
c SYS004 Systemic Mastocytosis 63 0.032
240
P MVM001 Movement Disease 63 0.032
241
TRN015 Transient Cerebral Ischemia 63 0.032
242
ANR007 Anorexia Nervosa 63 0.032
243
c GLC092 Glaucoma, Primary Open Angle 62 0.032
244
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.032
245
c LCL006 Localized Scleroderma 62 0.032
246
CLT003 Colitis 62 0.032
247
P PSR002 Psoriasis 62 0.032
248
c MLN065 Melanocytic Nevus Syndrome, Congenital 62 0.032
249
P ART023 Arthropathy 62 0.032
250
ALL026 Allergic Hypersensitivity Disease 62 0.032
251
P PRM006 Primary Biliary Cirrhosis 62 0.032
252
LVR012 Liver Cirrhosis 62 0.032
253
MSL001 Measles 62 0.032
254
P PRP029 Porphyria 62 0.032
255
CHL068 Cholestasis 61 0.032
256
INT002 Intermittent Claudication 61 0.032
257
c SCL052 Scleroderma, Familial Progressive 61 0.032
258
P MYL006 Myeloid Leukemia 60 0.032
259
P BNG030 Benign Ependymoma 60 0.032
260
c ACT027 Acute Pancreatitis 60 0.032
261
ACQ007 Acquired Immunodeficiency Syndrome 60 0.032
262
SQM006 Squamous Cell Carcinoma 60 0.032
263
P SNS001 Sensorineural Hearing Loss 60 0.032
264
VRC005 Varicose Veins 60 0.032
265
P CTR002 Cataract 60 0.032
266
STT001 Status Epilepticus 60 0.032
267
P OPT006 Optic Nerve Disease 60 0.032
268
PBL005 Piebald Trait 59 0.032
269
P MCR010 Microcephaly 59 0.032
270
VSL002 Visual Epilepsy 59 0.032
271
P WRD001 Waardenburg's Syndrome 59 0.032
272
CYS010 Cystinosis 59 0.032
273
ALP097 Alopecia Universalis Congenita 59 0.032
274
PPT005 Peptic Ulcer Disease 59 0.032
275
P SYP003 Syphilis 58 0.032
276
P STR022 Stargardt Disease 58 0.032
277
c PRG018 Paragangliomas 1 58 0.032
278
CCC001 Coccidioidomycosis 58 0.032
279
PLM026 Pilomatrixoma 58 0.032
280
P URT039 Urticaria 58 0.032
281
MNT002 Mental Depression 58 0.032
282
P CND004 Candidiasis 58 0.032
283
P INF032 Infertility 57 0.032
284
BRN056 Bronchopulmonary Dysplasia 57 0.032
285
P RHN004 Rhinitis 57 0.032
286
P HDC001 Headache 57 0.032
287
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.032
288
c LKM070 Leukemia, Acute Monocytic 57 0.032
289
P BPL003 Bipolar Disorder 56 0.032
290
PPL058 Papilloma of Choroid Plexus 56 0.032
291
EXF001 Exfoliation Syndrome 56 0.032
292
BCT022 Bacterial Infectious Disease 56 0.032
293
P SZR006 Seizure Disorder 56 0.032
294
ISL001 Islet Cell Tumor 56 0.032
295
NRL004 Neuroleptic Malignant Syndrome 56 0.032
296
HPT022 Hepatoblastoma 56 0.032
297
HST011 Histoplasmosis 55 0.032
298
FND002 Fundus Dystrophy 55 0.032
299
P DRR001 Diarrhea 55 0.032
300
P SBS003 Substance Abuse 55 0.032
301
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.032
302
SJG002 Sjogren-Larsson Syndrome 54 0.032
303
GLC003 Glucose Intolerance 54 0.032
304
GNG004 Ganglioglioma 54 0.032
305
CLL010 Cellular Ependymoma 54 0.032
306
DBT010 Diabetic Neuropathy 54 0.032
307
c PST005 Posterior Uveitis 54 0.032
308
PPL022 Papilloma 54 0.032
309
SLP001 Sleeping Sickness 54 0.032
310
P END047 Endophthalmitis 53 0.032
311
P MNC007 Monocytic Leukemia 53 0.032
312
ACR014 Acral Lentiginous Melanoma 53 0.032
313
OCL006 Ocular Hypertension 53 0.032
314
GST023 Gastric Ulcer 53 0.032
315
c WRD033 Waardenburg Syndrome, Type 2e 53 0.032
316
c GLL024 Gallbladder Disease 1 53 0.032
317
P ANT088 Anterior Segment Dysgenesis 52 0.032
318
DMY004 Demyelinating Disease 52 0.032
319
P PRG013 Paraganglioma 52 0.032
320
PST011 Pustulosis of Palm and Sole 52 0.032
321
P DDN001 Duodenal Ulcer 52 0.032
322
IMP005 Impotence 52 0.032
323
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 52 0.032
324
PTH003 Pathologic Nystagmus 52 0.032
325
ACT200 Acute Monoblastic Leukemia 52 0.032
326
TLN003 Telangiectasis 52 0.032
327
ONC002 Onchocerciasis 52 0.032
328
c INH030 Inherited Retinal Disorder 51 0.032
329
SPS003 Spastic Diplegia 51 0.032
330
c ALB020 Albinism, Oculocutaneous, Type Iii 51 0.032
331
P HYP077 Hypertrichosis 50 0.032
332
PLR007 Pleural Empyema 50 0.032
333
SCB001 Scabies 50 0.032
334
CHL122 Cholesteatoma of Middle Ear 50 0.032
335
CHR078 Chorioretinitis 50 0.032
336
TRY001 Trypanosomiasis 50 0.032
337
P OBS001 Obstructive Jaundice 50 0.032
338
BLS002 Blastomycosis 50 0.032
339
IRR003 Irritant Dermatitis 49 0.032
340
MNN009 Meningoencephalitis 49 0.032
341
QDR001 Quadriplegia 48 0.032
342
P NGH001 Night Blindness 48 0.032
343
PRS012 Pars Planitis 48 0.032
344
c ALB019 Albinism, Oculocutaneous, Type Iv 48 0.032
345
MDD010 Middle Ear Disease 48 0.032
346
THY128 Thyroid Tumor 47 0.032
347
c INH020 Inherited Metabolic Disorder 47 0.032
348
STM006 Stomach Disease 47 0.032
349
RTN020 Retinal Vascular Disease 46 0.032
350
KRT013 Keratolytic Winter Erythema 46 0.032
351
AND014 Androgenic Alopecia 46 0.032
352
SQM002 Squamous Cell Papilloma 46 0.032
353
c HRM009 Hermansky-Pudlak Syndrome 6 45 0.032
354
ORL013 Oral Lichen Planus 45 0.032
355
SPP008 Suppurative Otitis Media 45 0.032
356
P SBR004 Seborrheic Dermatitis 45 0.032
357
P SDR002 Siderosis 44 0.032
358
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.032
359
P END039 Endodermal Sinus Tumor 44 0.032
360
GNG003 Gingival Recession 44 0.032
361
NDL001 Nodular Malignant Melanoma 44 0.032
362
ART006 Arthus Reaction 44 0.032
363
c SPH013 Spherocytosis, Type 1 44 0.032
364
MTR010 Mature Teratoma 44 0.032
365
P PRM001 Primary Cutaneous Amyloidosis 44 0.032
366
CLP005 Ciliopathy 43 0.032
367
c HRM012 Hermansky-Pudlak Syndrome 9 43 0.032
368
MST019 Mastoiditis 43 0.032
369
HYP084 Hypopyon 43 0.032
370
LWC001 Low Compliance Bladder 43 0.032
371
P HRD018 Hair Disease 43 0.032
372
P HYP265 Hypotonia 43 0.032
373
P MJR007 Major Affective Disorder 1 43 0.032
374
MST004 Mast Cell Neoplasm 42 0.032
376
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.032
377
c PST022 Posterior Uveal Melanoma 42 0.032
378
PLM020 Pleomorphic Xanthoastrocytoma 41 0.032
379
c AMY060 Amyloidosis, Primary Localized Cutaneous, 1 41 0.032
380
ANX004 Anoxia 40 0.032
381
CNN010 Connective Tissue Benign Neoplasm 40 0.032
382
FNG016 Fungal Keratitis 40 0.032
383
AML004 Ameloblastic Carcinoma 39 0.032
384
PRP002 Periapical Granuloma 39 0.032
385
TST018 Testicular Yolk Sac Tumor 39 0.032
386
EXT007 Extracutaneous Mastocytoma 38 0.032
387
ALL014 Allergic Encephalomyelitis 38 0.032
388
PTY002 Pityriasis Versicolor 38 0.032
389
BTN004 Biotin Deficiency 38 0.032
390
ACN010 Acanthoma 38 0.032
391
MLN003 Melancholia 38 0.032
392
SRT002 Sertoli Cell Tumor 38 0.032
393
EMB002 Embryoma 38 0.032
394
PRV003 Perivascular Epithelioid Cell Tumor 37 0.032
395
EPD070 Epidermoid Cysts 37 0.032
396
c BNG093 Benign Teratoma 37 0.032
397
c NGH027 Night Blindness, Congenital Stationary, Type 1c 37 0.032
398
ECC002 Eccrine Acrospiroma 36 0.032
399
HRW001 Hair Whorl 36 0.032
400
SPT022 Spitzoid Melanoma 36 0.032
401
c ALB016 Albinism, Oculocutaneous, Type Vii 35 0.032
402
c HRM011 Hermansky-Pudlak Syndrome 8 35 0.032
403
CYC001 Cycloplegia 35 0.032
404
EMY001 Eumycotic Mycetoma 34 0.032
405
HNS001 Hansen's Disease 34 0.032
406
MLG061 Malignant Choroid Melanoma 34 0.032
407
STC004 Stachybotrys Chartarum 34 0.032
408
P CLR001 Clear Cell Acanthoma 34 0.032
409
SBC019 Subcutaneous Mycosis 34 0.032
410
MLN001 Melanotic Neuroectodermal Tumor 33 0.032
411
GNT167 Genetic Obesity 33 0.032
412
ADN014 Adenomatoid Tumor 33 0.032
413
LNT002 Lentigo Maligna Melanoma 33 0.032
414
c CHR097 Chronic Purulent Otitis Media 33 0.032
415
c MJR003 Major Affective Disorder 6 33 0.032
416
c MJR006 Major Affective Disorder 5 33 0.032
417
PGM002 Pigmented Basal Cell Carcinoma 32 0.032
418
IDP031 Idiopathic Hypersomnia 32 0.032
419
c AMY111 Amyloidosis, Primary Localized Cutaneous, 3 32 0.032
420
PHT003 Phototoxic Dermatitis 31 0.032
421
MLN004 Melanotic Medulloblastoma 31 0.032
422
P DYS023 Dyschromatosis Universalis Hereditaria 31 0.032
423
OVR121 Ovarian Sex-Cord Stromal Tumor 31 0.032
424
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.032
425
OVR017 Ovarian Cystic Teratoma 28 0.032
426
PHS025 Phosphatase, Acid, of Tissues 28 0.032
427
HLN001 Halo Nevi 27 0.032
428
ECT089 Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia 27 0.032
429
NRN022 Neurenteric Cyst 26 0.032
430
LCH008 Lichen Planus Pigmentosus 24 0.032
431
SCL011 Sclerosing Keratitis 23 0.032
432
c DWL003 Dowling-Degos Disease 2 22 0.032
433
RTN173 Retinal Dystrophy and Obesity 22 0.032
434
LNT008 Lentiginosis, Inherited Patterned 21 0.032
435
P ACT046 Acute Apical Periodontitis 21 0.032
436
MCL047 Macular Amyloidosis 21 0.032
437
PHC015 Phacoanaphylactic Uveitis 19 0.032
438
TNG011 Tongue, Pigmented Fungiform Papillae of 8 0.032
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