Search results for Acitretin

301 hits were found for Acitretin

# Family MCID Name MIFTS Score
1
ACT091 Acitretin Embryopathy 7 5.510
2
ACT206 Acitretin/etretinate Embryopathy 18 3.930
3
P PSR002 Psoriasis 62 0.552
4
PST011 Pustulosis of Palm and Sole 52 0.551
5
c PSR028 Psoriasis 7 42 0.235
6
c PSR017 Psoriasis 2 53 0.232
7
c PSR023 Psoriasis 1 52 0.232
8
c PSR032 Psoriasis 11 47 0.232
9
c PSR018 Psoriasis 13 41 0.232
10
KRT009 Keratosis 51 0.209
11
P ICH004 Ichthyosis 54 0.206
12
P LCH002 Lichen Planus 53 0.199
13
P PST059 Pustular Psoriasis 37 0.184
14
P SKN015 Skin Carcinoma 66 0.164
15
P ALP008 Alopecia 54 0.164
16
SQM006 Squamous Cell Carcinoma 60 0.155
17
PLM029 Palmoplantar Keratosis 47 0.150
18
SKN016 Skin Disease 63 0.136
19
c PSR021 Psoriasis 14, Pustular 50 0.136
20
P PTY003 Pityriasis Rubra Pilaris 58 0.125
21
CHL056 Cheilitis 48 0.125
22
c BSL007 Basal Cell Carcinoma 68 0.119
23
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.119
24
P KRT005 Keratoacanthoma 48 0.119
25
DRM006 Dermatitis 61 0.113
26
c NRF023 Neurofibromatosis, Type Ii 80 0.106
27
HDR002 Hidradenitis Suppurativa 55 0.106
28
HDR003 Hidradenitis 49 0.106
29
P HYP058 Hypervitaminosis a 48 0.106
30
P LPS004 Lupus Erythematosus 61 0.099
31
SKN022 Skin Squamous Cell Carcinoma 57 0.099
32
P CTN015 Cutaneous T Cell Lymphoma 49 0.099
33
IMM167 Immune Deficiency Disease 78 0.092
34
P AMY004 Amyloidosis 70 0.092
35
MYC006 Mycosis Fungoides 66 0.092
36
c BSL024 Basal Cell Carcinoma 1 56 0.092
37
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.092
38
LPD016 Lipoid Proteinosis of Urbach and Wiethe 50 0.092
39
SBC012 Subcorneal Pustular Dermatosis 43 0.092
40
ACR005 Acrodermatitis 38 0.092
41
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.092
42
P ALZ034 Alzheimer Disease 88 0.084
43
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.084
44
KRT019 Keratitis, Hereditary 65 0.084
45
PPL049 Papillon-Lefevre Syndrome 65 0.084
46
c BRN108 Branchiootic Syndrome 1 62 0.084
47
P HYP750 Hypertriglyceridemia, Familial 62 0.084
48
P ALP009 Alopecia Areata 60 0.084
49
P PRK001 Porokeratosis 55 0.084
50
P NLD001 Nail Disease 54 0.084
51
SKN013 Skin Benign Neoplasm 51 0.084
52
ATS010 Autosomal Recessive Disease 48 0.084
53
LCH014 Lichen Amyloidosis 31 0.084
54
BSL036 Basal Cell Nevus Syndrome 73 0.075
55
HMN044 Human Immunodeficiency Virus Type 1 71 0.075
56
DFC004 Deficiency Anemia 70 0.075
57
P LKM002 Leukemia 68 0.075
58
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.075
59
P CNJ013 Conjunctivitis 65 0.075
60
PSR001 Psoriatic Arthritis 61 0.075
61
c BNG091 Benign Chronic Pemphigus 58 0.075
62
P EPD083 Epidermodysplasia Verruciformis 1 58 0.075
63
c DWL002 Dowling-Degos Disease 1 58 0.075
64
P EXN002 Exanthem 57 0.075
65
P ERY053 Erythrokeratodermia Variabilis Et Progressiva 1 57 0.075
66
EPD002 Epidermolytic Hyperkeratosis 56 0.075
67
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.075
68
P PMP001 Pemphigus 54 0.075
69
PPL022 Papilloma 54 0.075
70
c ICH069 Ichthyosis, Congenital, Autosomal Recessive 4b 51 0.075
71
BLP005 Blepharitis 50 0.075
72
PYD002 Pyoderma 50 0.075
73
BLS002 Blastomycosis 50 0.075
74
P PHT010 Photoparoxysmal Response 1 42 0.075
75
LCH016 Lichen Sclerosus Et Atrophicus 41 0.075
76
ACT011 Acute Contagious Conjunctivitis 40 0.075
77
48X005 48,xyyy 39 0.075
78
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 38 0.075
79
c ERY062 Erythrokeratodermia Variabilis Et Progressiva 5 23 0.075
80
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.065
81
P MLN008 Melanoma 69 0.065
82
P ART022 Arthritis 69 0.065
83
P LYM118 Lymphoma 68 0.065
84
P LVR013 Liver Disease 68 0.065
85
SKN019 Skin Melanoma 68 0.065
86
P PRD008 Periodontitis 64 0.065
87
LPD008 Lipid Metabolism Disorder 62 0.065
88
ACN002 Acanthosis Nigricans 60 0.065
89
ACQ007 Acquired Immunodeficiency Syndrome 60 0.065
90
DRR014 Darier-White Disease 60 0.065
91
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.065
92
P URT039 Urticaria 58 0.065
93
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.065
94
P ANG015 Angioedema 57 0.065
95
c FML035 Familial Hyperlipidemia 55 0.065
96
P CTN003 Cutaneous Lupus Erythematosus 53 0.065
97
INT075 Intracranial Hypertension 53 0.065
98
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.065
99
RSD004 Rosai-Dorfman Disease 51 0.065
100
VRR004 Verrucous Carcinoma 49 0.065
101
KRT013 Keratolytic Winter Erythema 46 0.065
102
c PRM038 Primary Agammaglobulinemia 44 0.065
103
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.065
104
49X006 49, Xxxxy Syndrome 41 0.065
105
PYG006 Pyogenic Granuloma 41 0.065
106
BWN006 Bowen's Disease 32 0.065
107
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.065
108
IGP001 Iga Pemphigus 26 0.065
109
GNR033 Generalized Eruptive Keratoacanthoma 22 0.065
110
c SPN225 Spondyloarthropathy 1 73 0.053
111
P NRB001 Neuroblastoma 72 0.053
112
P MYP004 Myopathy 70 0.053
113
P HYP086 Hypothyroidism 69 0.053
114
NVS017 Nevus, Epidermal 68 0.053
115
P HPT021 Hepatitis 67 0.053
116
P FLL037 Follicular Lymphoma 67 0.053
117
P HYP098 Hypereosinophilic Syndrome 67 0.053
118
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.053
119
PLG002 Plague 63 0.053
120
P ECT006 Ectodermal Dysplasia 62 0.053
121
BLL006 Bullous Pemphigoid 62 0.053
122
P VSC011 Vasculitis 62 0.053
123
CHN055 Chanarin-Dorfman Syndrome 61 0.053
124
c ACT027 Acute Pancreatitis 60 0.053
125
P SNS001 Sensorineural Hearing Loss 60 0.053
126
P ANP001 Anaplastic Large Cell Lymphoma 58 0.053
127
P PRP019 Peripheral Nervous System Disease 58 0.053
128
LNG108 Langerhans Cell Histiocytosis 58 0.053
129
P RHN004 Rhinitis 57 0.053
130
INT303 Intracranial Hypertension, Idiopathic 57 0.053
131
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.053
132
P NRP001 Neuropathy 56 0.053
133
P PLY019 Polyneuropathy 56 0.053
134
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.053
135
CPL003 Capillary Leak Syndrome 55 0.053
136
SJG002 Sjogren-Larsson Syndrome 54 0.053
137
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 53 0.053
138
ICH054 Ichthyosis, X-Linked 53 0.053
139
PNM005 Pneumonic Plague 51 0.053
140
SCB001 Scabies 50 0.053
141
HRT011 Heart Septal Defect 50 0.053
142
47X002 47,xyy 49 0.053
143
HST010 Histiocytosis 48 0.053
144
HYP068 Hyperostosis 48 0.053
145
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.053
146
KRT002 Keratomalacia 47 0.053
147
P ARR027 Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 47 0.053
148
SQM002 Squamous Cell Papilloma 46 0.053
149
PNT038 Peanut Allergy 45 0.053
150
BZX001 Bazex Syndrome 45 0.053
151
MLD006 Mal De Meleda 44 0.053
152
DSC009 Discoid Lupus Erythematosus 42 0.053
153
P ECT005 Ectropion 42 0.053
154
ELP001 Elephantiasis 41 0.053
155
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.053
156
ACR004 Acrokeratosis Verruciformis 38 0.053
157
ABD002 Abducens Nerve Disease 37 0.053
158
NRW001 Norwegian Scabies 37 0.053
159
HMM002 Haim-Munk Syndrome 36 0.053
160
LNR004 Linear Porokeratosis 34 0.053
161
LCH013 Lichen Planus Pemphigoides 34 0.053
162
LCH003 Lichen Nitidus 31 0.053
163
c PSR024 Psoriasis 3 28 0.053
164
PSD026 Pseudoainhum 27 0.053
165
CHL079 Children's Interstitial Lung Disease 26 0.053
166
DFF010 Diffuse Alopecia Areata 26 0.053
167
P PNC113 Punctate Palmoplantar Keratoderma 24 0.053
168
STR067 Stroke, Ischemic 81 0.038
169
P OST002 Osteoporosis 74 0.038
170
c HYP836 Hypercholesterolemia, Familial, 1 73 0.038
171
ANX010 Anxiety 73 0.038
172
P GRF003 Graft-Versus-Host Disease 72 0.038
173
DWN001 Down Syndrome 70 0.038
174
P PNM007 Pneumonia 68 0.038
175
CST001 Costello Syndrome 68 0.038
176
P MYS003 Myasthenia Gravis 68 0.038
177
P THR014 Thrombocytopenia 67 0.038
178
P PSD087 Pseudoxanthoma Elasticum 65 0.038
179
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.038
180
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.038
181
CLF027 Cleft Palate, Isolated 64 0.038
182
P ANR048 Aniridia 1 63 0.038
183
ACT119 Acute Promyelocytic Leukemia 63 0.038
184
ANR007 Anorexia Nervosa 63 0.038
185
DPR016 Depression 63 0.038
186
c LCL006 Localized Scleroderma 62 0.038
187
c HPT003 Hepatitis a 62 0.038
188
P TRC086 Trichohepatoenteric Syndrome 1 62 0.038
189
ATM095 Autoimmune Disease 62 0.038
190
LVR012 Liver Cirrhosis 62 0.038
191
CHL068 Cholestasis 61 0.038
192
HYP066 Hyperglycemia 61 0.038
193
P PNC044 Pancreatitis 61 0.038
194
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.038
195
P ATR010 Atrial Heart Septal Defect 60 0.038
196
MRT001 Muir-Torre Syndrome 60 0.038
197
P MCR010 Microcephaly 59 0.038
198
c PCH015 Pachyonychia Congenita 1 59 0.038
199
IGR001 Ige Responsiveness, Atopic 59 0.038
200
GNG013 Gingivitis 59 0.038
201
P SYP003 Syphilis 58 0.038
202
P ALC033 Alcohol Use Disorder 58 0.038
203
P CND004 Candidiasis 58 0.038
204
P GLM007 Glomerulonephritis 57 0.038
205
c CHR417 Chronic Graft Versus Host Disease 57 0.038
206
c ACT134 Acute Liver Failure 56 0.038
207
BCT022 Bacterial Infectious Disease 56 0.038
208
MCS002 Mucositis 56 0.038
209
MCL006 Macular Retinal Edema 55 0.038
210
P ATR001 Atrioventricular Septal Defect 55 0.038
211
RSC001 Rosacea 54 0.038
212
THR013 Thoracic Outlet Syndrome 54 0.038
213
SNS003 Sensory Peripheral Neuropathy 54 0.038
214
P ACT008 Actinic Keratosis 53 0.038
215
PRP016 Paraplegia 52 0.038
216
IMP005 Impotence 52 0.038
217
OCL069 Ocular Motor Apraxia 51 0.038
218
P VHW001 Vohwinkel Syndrome 51 0.038
219
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.038
220
P HYP077 Hypertrichosis 50 0.038
221
LNT004 Lentigines 50 0.038
222
c HRD202 Hereditary Lymphedema I 50 0.038
223
P KRT007 Keratoconus 50 0.038
224
HYP080 Hypogonadism 50 0.038
225
FRN020 Frontal Fibrosing Alopecia 49 0.038
226
MNL001 Monilethrix 48 0.038
227
BNR002 Bone Resorption Disease 48 0.038
228
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 0.038
229
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.038
230
BNN003 Bone Inflammation Disease 48 0.038
231
SXL003 Sexual Disorder 47 0.038
232
CHR031 Chromoblastomycosis 47 0.038
233
MLT152 Multiple Self-Healing Squamous Epithelioma 47 0.038
234
KRT008 Keratopathy 47 0.038
235
FLL008 Folliculitis 46 0.038
236
ORL013 Oral Lichen Planus 45 0.038
237
SPS057 Spasticity 45 0.038
238
GRN017 Granulocytopenia 44 0.038
239
TNG009 Tongue Squamous Cell Carcinoma 44 0.038
240
GRN007 Granuloma Annulare 44 0.038
241
P PRM001 Primary Cutaneous Amyloidosis 44 0.038
242
AND001 Anodontia 43 0.038
243
SKN005 Skin Atrophy 43 0.038
244
HYP084 Hypopyon 43 0.038
245
SDD008 Sudden Sensorineural Hearing Loss 43 0.038
246
HYP457 Hypertrophic Scars 42 0.038
247
CYT002 Cytokine Deficiency 42 0.038
248
P CRN035 Cranial Nerve Palsy 42 0.038
249
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.038
250
P HYP087 Hypotrichosis 42 0.038
251
c AMY060 Amyloidosis, Primary Localized Cutaneous, 1 41 0.038
252
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.038
253
RTR011 Retroperitoneal Fibrosis 40 0.038
254
ERY061 Erythroderma, Congenital, with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-Ige 39 0.038
255
c CHR682 Chronic Bilirubin Encephalopathy 39 0.038
256
NTR042 Neutrophilic Dermatosis, Acute Febrile 38 0.038
257
PTY002 Pityriasis Versicolor 38 0.038
258
LYM052 Lymphomatoid Papulosis 38 0.038
259
P SYR003 Syringoma 37 0.038
260
BLN010 Balanitis 37 0.038
261
ACR062 Acroosteolysis 35 0.038
262
ATX010 Ataxia Neuropathy Spectrum 34 0.038
263
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 34 0.038
264
INF057 Inflammatory Linear Verrucous Epidermal Nevus 34 0.038
265
BWN003 Bowenoid Papulosis 34 0.038
266
ACT064 Acute Necrotizing Encephalitis 33 0.038
267
KNC002 Knuckle Pads 33 0.038
268
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.038
269
GTT002 Guttate Psoriasis 32 0.038
270
c AMY111 Amyloidosis, Primary Localized Cutaneous, 3 32 0.038
271
FLL019 Follicular Mucinosis 31 0.038
272
BLP006 Blepharoconjunctivitis 31 0.038
273
INT065 Interstitial Keratitis 30 0.038
274
c ICH023 Ichthyosis, Acquired 30 0.038
275
ELS002 Elastosis Perforans Serpiginosa 30 0.038
276
GRV012 Grover's Disease 30 0.038
277
STR096 Striate Palmoplantar Keratoderma 29 0.038
278
HRD216 Hereditary Palmoplantar Keratoderma 28 0.038
279
GRN032 Granulomatous Slack Skin Disease 28 0.038
280
ANH001 Ainhum 27 0.038
281
c FML223 Familial Keratoacanthoma 26 0.038
282
ESN016 Eosinophilic Pustular Folliculitis 25 0.038
283
c PSR027 Psoriasis 6 25 0.038
284
LCH008 Lichen Planus Pigmentosus 24 0.038
285
LLS001 Lelis Syndrome 24 0.038
286
c ALP099 Alopecia, Congenital 23 0.038
287
ERS002 Erosive Pustular Dermatosis of the Scalp 23 0.038
288
KYR001 Kyrle Disease 23 0.038
289
RRG043 Rare Genetic Skin Disease 22 0.038
290
ATR052 Atrophic Lichen Planus 21 0.038
291
BLL015 Bullous Lichen Planus 21 0.038
292
IST006 Isotretinoin Syndrome 20 0.038
293
c CHR686 Chronic Cutaneous Lupus Erythematosus 19 0.038
294
BLD137 Blood Group--Ahonen 16 0.038
295
c CNG596 Congenital Ectropion 16 0.038
296
HDR007 Hidrotic Ectodermal Dysplasia 2 16 0.038
297
FCL040 Focal Acral Hyperkeratosis 15 0.038
298
ANN013 Annular Atrophic Lichen Planus 14 0.038
299
ACR120 Acrokeratoderma 14 0.038
300
VLV006 Vulva Verrucous Carcinoma 9 0.038
301
P RRH006 Rare Hyperlipidemia 6 0.038
Content
Loading form....