Search results for Aminolevulinic acid

372 hits were found for Aminolevulinic acid

# Family MCID Name MIFTS Score
1
AMN017 Aminolevulinic Acid Dehydratase Deficiency Porphyria 7 2.797
2
AMN008 Aminolevulinate Dehydratase Deficiency Porphyria 5 2.770
3
KRT009 Keratosis 51 0.348
4
P PRP029 Porphyria 62 0.332
5
P ACT008 Actinic Keratosis 53 0.320
6
c NRF023 Neurofibromatosis, Type Ii 80 0.298
7
P LVR013 Liver Disease 68 0.279
8
c BSL007 Basal Cell Carcinoma 68 0.273
9
48X005 48,xyyy 39 0.264
10
GLL048 Glial Tumor 45 0.256
11
P GLM045 Glioma 63 0.254
12
FTT001 Fatty Liver Disease 61 0.243
13
LVR012 Liver Cirrhosis 62 0.241
14
P NRB001 Neuroblastoma 72 0.237
15
P SZR006 Seizure Disorder 56 0.235
16
P SKN015 Skin Carcinoma 66 0.233
17
GLB015 Glioblastoma Multiforme 75 0.230
18
VSL002 Visual Epilepsy 59 0.229
19
P KDN018 Kidney Disease 72 0.228
20
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.228
21
P CLR023 Colorectal Cancer 99 0.218
22
P BLD134 Bladder Cancer 79 0.215
23
HLX001 Helix Syndrome 47 0.213
24
PRP083 Porphyria, Acute Intermittent 64 0.205
25
DFC004 Deficiency Anemia 70 0.204
26
P PSR002 Psoriasis 62 0.204
27
DRM006 Dermatitis 61 0.203
28
PST011 Pustulosis of Palm and Sole 52 0.202
29
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.198
30
P BRS047 Breast Cancer 97 0.194
31
c FNC043 Fanconi Anemia, Complementation Group E 62 0.193
32
HYP066 Hyperglycemia 61 0.191
33
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.190
34
P ADN016 Adenocarcinoma 64 0.186
35
P LKM002 Leukemia 68 0.183
36
BWN006 Bowen's Disease 32 0.180
37
CLT003 Colitis 62 0.178
38
P HPT023 Hepatocellular Carcinoma 100 0.178
39
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.177
40
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.176
41
IRN002 Iron Metabolism Disease 57 0.174
42
ATH013 Atherosclerosis Susceptibility 65 0.170
43
c MLG068 Malignant Glioma 46 0.170
44
SKN016 Skin Disease 63 0.168
45
SQM006 Squamous Cell Carcinoma 60 0.168
46
P PRS040 Prostate Cancer 97 0.168
47
c RHB024 Rhabdomyosarcoma 2 67 0.166
48
ULC004 Ulcerative Colitis 73 0.164
49
P NRP001 Neuropathy 56 0.161
50
P TYR004 Tyrosinemia 58 0.161
51
ADN018 Adenoma 59 0.160
52
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.157
53
P ALZ034 Alzheimer Disease 88 0.156
54
SPR005 Superficial Basal Cell Carcinoma 46 0.155
55
BRN028 Brain Cancer 74 0.155
56
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.154
57
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.154
58
ATM095 Autoimmune Disease 62 0.152
59
OST159 Osteogenic Sarcoma 66 0.151
60
P AST007 Astrocytoma 51 0.150
61
P GLM040 Glioma Susceptibility 1 81 0.150
62
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.149
63
c ACT078 Acute Porphyria 51 0.148
64
ALC007 Alcohol Dependence 66 0.147
65
c DWL002 Dowling-Degos Disease 1 58 0.147
66
c PRC016 Pre-Eclampsia 63 0.147
67
HYP266 Hypoxia 57 0.144
68
P LNG032 Lung Cancer 98 0.143
69
P ESP024 Esophagitis 62 0.143
70
P INS002 in Situ Carcinoma 53 0.143
71
P PNC035 Pancreatic Cancer 84 0.142
72
P BRS044 Breast Adenocarcinoma 59 0.142
73
P DBT009 Diabetes Mellitus 64 0.141
74
P MLN008 Melanoma 69 0.140
75
P SDR003 Sideroblastic Anemia 49 0.140
76
BRR014 Barrett Esophagus 65 0.139
77
c PCH010 Pachyonychia Congenita 3 44 0.136
78
ERY051 Erythroleukemia, Familial 56 0.135
79
PPL052 Papillomatosis, Confluent and Reticulated 33 0.135
80
P PRP056 Porphyria, Acute Hepatic 48 0.134
81
NDL009 Nodular Basal Cell Carcinoma 43 0.133
82
URM002 Uremia 49 0.133
83
CNT047 Contact Dermatitis 58 0.132
84
P LYM118 Lymphoma 68 0.132
85
P FBR017 Fibrosarcoma 56 0.131
86
P HYP086 Hypothyroidism 69 0.130
87
P ATS364 Autism 70 0.129
88
47X002 47,xyy 49 0.129
89
CHL014 Cholera 59 0.129
90
CRH001 Crohn's Disease 74 0.127
91
AGN016 Aging 56 0.127
92
END086 End Stage Renal Disease 51 0.127
93
P BCL017 B-Cell Lymphoma 58 0.126
94
NTR005 Nutritional Deficiency Disease 62 0.126
95
P HRP006 Herpes Simplex 65 0.126
96
P TRN020 Turner Syndrome 67 0.126
97
P DRM053 Dermatitis, Atopic 66 0.123
98
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.123
99
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.123
100
CRB039 Cerebrovascular Disease 67 0.122
101
PPL022 Papilloma 54 0.122
102
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.121
103
CRV035 Cervical Cancer 76 0.121
104
RSC001 Rosacea 54 0.121
105
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.121
106
STR067 Stroke, Ischemic 81 0.121
107
P LTR001 Lateral Sclerosis 54 0.121
108
c BSL024 Basal Cell Carcinoma 1 56 0.120
109
c ATS007 Autism Spectrum Disorder 67 0.120
110
RCK004 Rickets 68 0.119
111
MXD026 Mixed Glioma 45 0.119
112
GLC003 Glucose Intolerance 54 0.119
113
MNN042 Meningioma, Radiation-Induced 62 0.118
114
DWN001 Down Syndrome 70 0.118
115
c MNN043 Meningioma, Familial 74 0.118
116
SPN021 Spinal Meningioma 50 0.117
117
SCR001 Secretory Meningioma 41 0.117
118
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.117
119
CHL056 Cheilitis 48 0.117
120
P LPS004 Lupus Erythematosus 61 0.115
121
HMP009 Haemophilus Influenzae 43 0.115
122
KRT013 Keratolytic Winter Erythema 46 0.114
123
ALL010 Allergic Contact Dermatitis 56 0.114
124
LSH001 Leishmaniasis 63 0.114
125
P KLZ004 Kala-Azar 1 41 0.114
126
c SYS001 Systemic Lupus Erythematosus 86 0.112
127
ADL002 Adult Syndrome 70 0.111
128
ATX019 Ataxia with Vitamin E Deficiency 42 0.111
129
SQM002 Squamous Cell Papilloma 46 0.110
130
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.110
131
CRV045 Cervical Intraepithelial Neoplasia 39 0.110
132
P PRP019 Peripheral Nervous System Disease 58 0.110
133
P SCH015 Schizophrenia 74 0.110
134
P PRP003 Porphyria Cutanea Tarda 67 0.109
135
P ALP008 Alopecia 54 0.109
136
IRN001 Iron Deficiency Anemia 59 0.108
137
ORL011 Oral Cancer 60 0.107
138
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.107
139
MMM001 Mammary Paget's Disease 53 0.107
140
P BNG032 Benign Mesothelioma 46 0.107
141
THY029 Thyroid Carcinoma 59 0.106
142
P ALC033 Alcohol Use Disorder 58 0.106
143
P SPP010 Suppressor of Tumorigenicity 3 51 0.106
144
GLS001 Gliosarcoma 54 0.106
145
P THL005 Thalassemia 60 0.106
146
P HPT021 Hepatitis 67 0.105
147
TLN003 Telangiectasis 52 0.104
148
c SML038 Small Cell Cancer of the Lung 65 0.104
149
c HPT001 Hepatitis C 62 0.103
150
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.103
151
GST033 Gestational Diabetes 61 0.103
152
P MLT020 Multiple Sclerosis 72 0.103
153
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.102
154
CLN015 Colon Adenocarcinoma 65 0.102
155
P CTN015 Cutaneous T Cell Lymphoma 49 0.102
156
P TRM003 Tremor 54 0.100
157
CHL065 Cholangiocarcinoma 68 0.100
158
ESP021 Esophageal Cancer 90 0.100
159
TRN018 Transitional Cell Carcinoma 56 0.099
160
MYC006 Mycosis Fungoides 66 0.099
161
P NSP012 Nasopharyngeal Carcinoma 66 0.099
162
INT079 Intrahepatic Cholangiocarcinoma 51 0.099
163
P LKM071 Leukemia, Chronic Lymphocytic 79 0.098
164
LKP003 Leukoplakia 39 0.098
165
P PLY019 Polyneuropathy 56 0.097
166
SKN013 Skin Benign Neoplasm 51 0.097
167
P PLM037 Pulmonary Hypertension 67 0.097
168
LYM019 Lymphosarcoma 46 0.096
169
ORL015 Oral Squamous Cell Carcinoma 43 0.096
170
HMS001 Hemosiderosis 54 0.094
171
ACT093 Actinic Cheilitis 40 0.094
172
SKN019 Skin Melanoma 68 0.093
173
PRN011 Pernicious Anemia 53 0.093
174
PNG002 Pain Agnosia 51 0.093
175
P RRH023 Rare Hereditary Hemochromatosis 41 0.092
176
LYM133 Lymphoma, Hodgkin, Classic 69 0.092
177
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.092
178
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.092
179
P OLG002 Oligodendroglioma 67 0.091
180
P MDL005 Medulloblastoma 77 0.091
181
c ACT134 Acute Liver Failure 56 0.091
182
GRD007 Grade Iii Astrocytoma 59 0.091
183
P PLY018 Polycythemia 56 0.090
184
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.089
185
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.089
186
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.089
187
P AMY004 Amyloidosis 70 0.087
188
ATS010 Autosomal Recessive Disease 48 0.087
189
P HML002 Hemolytic Anemia 63 0.087
190
ORL012 Oral Leukoplakia 39 0.087
191
c TYR012 Tyrosinemia, Type I 66 0.087
192
CTN007 Cutaneous Leishmaniasis 62 0.084
193
MLR004 Malaria 81 0.083
194
P URT039 Urticaria 58 0.083
195
LNT004 Lentigines 50 0.082
196
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.082
197
BRN005 Brain Glioblastoma Multiforme 34 0.081
198
SCK003 Sickle Cell Anemia 74 0.081
199
P GRF003 Graft-Versus-Host Disease 72 0.080
200
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.080
201
BSL036 Basal Cell Nevus Syndrome 73 0.080
202
c ANM036 Anemia, Sideroblastic, 1 57 0.080
203
P FNC004 Fanconi Syndrome 50 0.080
204
HVY002 Heavy Metal Poisoning 22 0.080
205
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.079
206
LNG031 Lung Benign Neoplasm 51 0.079
207
c BTT014 Beta-Thalassemia 74 0.079
208
P FNC034 Fanconi Renotubular Syndrome 2 40 0.079
209
FNG017 Fungal Infectious Disease 53 0.079
210
DYS073 Dysphagia 50 0.078
211
GNG013 Gingivitis 59 0.077
212
AMN003 Amnestic Disorder 54 0.077
213
PLM031 Poliomyelitis 64 0.077
214
SBC016 Subacute Delirium 44 0.076
215
PST092 Posttransplant Acute Limbic Encephalitis 29 0.076
216
FLL008 Folliculitis 46 0.075
217
PLC008 Placenta Disease 50 0.074
218
c SPN225 Spondyloarthropathy 1 73 0.073
219
SKN022 Skin Squamous Cell Carcinoma 57 0.073
220
PTT037 Pituitary Tumors 44 0.072
221
P TRC086 Trichohepatoenteric Syndrome 1 62 0.072
222
P LRY044 Larynx Cancer 55 0.072
223
CRH005 Crohn's Colitis 53 0.071
224
GNT002 Giant Cell Glioblastoma 50 0.071
225
CHR100 Chronic Ulcer of Skin 55 0.071
226
c GRV008 Graves Disease 1 56 0.071
227
BRN032 Brain Glioma 45 0.070
228
P ALP009 Alopecia Areata 60 0.070
229
HDR003 Hidradenitis 49 0.070
230
SZR001 Sezary's Disease 60 0.070
231
CHC001 Chickenpox 60 0.070
232
P BNG030 Benign Ependymoma 60 0.069
233
HDR002 Hidradenitis Suppurativa 55 0.069
234
VRL011 Viral Infectious Disease 61 0.068
235
CLL010 Cellular Ependymoma 54 0.068
236
c SVR005 Severe Pre-Eclampsia 50 0.067
237
P SBR004 Seborrheic Dermatitis 45 0.066
238
AYM001 Ayme-Gripp Syndrome 57 0.066
239
49X006 49, Xxxxy Syndrome 41 0.066
240
P PTT006 Pituitary Adenoma 55 0.066
241
P NRF002 Neurofibromatosis 56 0.066
242
BLD131 Bladder Urothelial Carcinoma 62 0.065
243
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.065
244
CNN005 Connective Tissue Disease 68 0.065
245
c INF071 Inflammatory Bowel Disease 1 67 0.065
246
CPR004 Coproporphyria, Hereditary 57 0.065
247
CNT033 Central Nervous System Cancer 47 0.064
248
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.064
249
c PSR017 Psoriasis 2 53 0.064
250
c PSR023 Psoriasis 1 52 0.064
251
c PSR032 Psoriasis 11 47 0.064
252
c PSR028 Psoriasis 7 42 0.064
253
c PSR018 Psoriasis 13 41 0.064
254
c CHR682 Chronic Bilirubin Encephalopathy 39 0.062
255
c HMC039 Hemochromatosis, Type 1 74 0.062
256
GLB001 Gilbert Syndrome 58 0.062
257
ANG005 Anogenital Venereal Wart 55 0.061
258
PPL001 Papillary Adenoma 44 0.060
259
c MST023 Mesothelioma, Malignant 57 0.060
260
ERY023 Erythroplakia 24 0.060
261
NRF007 Neurofibroma 64 0.060
262
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.060
263
RDN001 Reading Disorder 40 0.060
264
c MLG084 Malignant Fibrous Histiocytoma 63 0.059
265
ORL006 Oral Mucosa Leukoplakia 23 0.059
266
P KRT005 Keratoacanthoma 48 0.059
267
RFR010 Refractory Anemia 48 0.058
268
HYP457 Hypertrophic Scars 42 0.058
269
KLD004 Keloid Disorder 40 0.058
270
P BRN035 Brain Stem Glioma 52 0.058
271
DRM011 Dermatophytosis 52 0.058
272
P ORL007 Oral Cavity Cancer 53 0.057
273
HYP080 Hypogonadism 50 0.057
274
TRP009 Triple X Syndrome 42 0.056
275
P MST009 Mastocytosis 64 0.056
276
P PRK001 Porokeratosis 55 0.056
277
MYL031 Myeloproliferative Neoplasm 66 0.056
278
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.056
279
P ANG001 Angelman Syndrome 69 0.055
280
P GLL022 Guillain-Barre Syndrome 59 0.055
281
c NRF024 Neurofibromatosis, Type I 77 0.055
282
INP001 Inappropriate Adh Syndrome 49 0.055
283
HRP004 Herpes Zoster 60 0.055
284
c ESS001 Essential Tremor 56 0.054
285
c MLG079 Malignant Pleural Mesothelioma 42 0.054
286
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.053
287
HYP082 Hypopharynx Cancer 47 0.053
288
c FNC026 Fanconi Renotubular Syndrome 1 39 0.053
289
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.053
290
ERS002 Erosive Pustular Dermatosis of the Scalp 23 0.053
291
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.052
292
P PHT010 Photoparoxysmal Response 1 42 0.052
293
BRN014 Bronchopneumonia 54 0.052
294
GLB024 Global Developmental Delay, Lung Cysts, Overgrowth, and Wilms Tumor 32 0.052
295
c SBR001 Seborrheic Infantile Dermatitis 30 0.052
296
XLN067 X-Linked Protoporphyria 16 0.052
297
CRV040 Cervix Carcinoma 51 0.051
298
HYL004 Hyaline Fibromatosis Syndrome 67 0.051
299
ORP003 Oropharynx Cancer 55 0.051
300
NCR002 Necrobiosis Lipoidica 38 0.050
301
HML018 Homologous Wasting Disease 22 0.050
302
P HYP024 Hypoparathyroidism 56 0.049
303
SXL003 Sexual Disorder 47 0.049
304
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.049
305
VRG001 Variegate Porphyria 56 0.048
306
VLV044 Vulvar Intraepithelial Neoplasia 44 0.048
307
c CHR417 Chronic Graft Versus Host Disease 57 0.047
308
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.047
309
ADN027 Adenomyosis 56 0.046
310
LCH016 Lichen Sclerosus Et Atrophicus 41 0.046
311
NRM004 Neuroma 51 0.045
312
c FML324 Familial Porphyria Cutanea Tarda 31 0.045
313
MXD011 Mixed Astrocytoma-Ependymoma 8 0.045
314
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.045
315
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.044
316
GRN007 Granuloma Annulare 44 0.044
317
FBR019 Fibromatosis 41 0.044
318
P NSL008 Nasal Cavity Cancer 41 0.043
319
CTN011 Cutaneous Porphyria 38 0.043
320
BWN003 Bowenoid Papulosis 34 0.043
321
PRT094 Protoporphyria, Erythropoietic, X-Linked 31 0.043
322
c HYP365 Hyperphenylalaninemia, Bh4-Deficient, D 31 0.043
323
LPN002 Lip and Oral Cavity Cancer 19 0.043
324
ANM041 Anemia, Nonspherocytic Hemolytic, Possibly Due to Defect in Porphyrin Metabolism 8 0.043
325
DBN001 Dubin-Johnson Syndrome 59 0.043
326
ANS011 Anus Cancer 56 0.043
327
c TYR013 Tyrosinemia, Type Ii 47 0.043
328
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.043
329
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.043
330
P FBR003 Fibrous Histiocytoma 44 0.043
331
P RRT020 Rare Tumor 41 0.043
332
PGM030 Pigmentation Anomaly of the Skin 26 0.043
333
c MLN065 Melanocytic Nevus Syndrome, Congenital 62 0.042
334
P CTN003 Cutaneous Lupus Erythematosus 53 0.042
335
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.041
336
DSM004 Desmoid Tumor 64 0.040
337
PTT009 Pituitary Gland Disease 54 0.040
338
VRR004 Verrucous Carcinoma 49 0.040
339
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.039
340
ACS001 Acoustic Neuroma 56 0.039
341
NVS017 Nevus, Epidermal 68 0.038
342
PRM126 Primary Peritoneal Carcinoma 62 0.038
343
PRN014 Paronychia 49 0.038
344
LNT002 Lentigo Maligna Melanoma 33 0.038
345
c BNG091 Benign Chronic Pemphigus 58 0.037
346
PRP082 Porphyria, Congenital Erythropoietic 56 0.037
347
DSM003 Desmoid Disease, Hereditary 48 0.037
348
MCR018 Microcytic Anemia 47 0.037
349
ANL022 Anal Fistula 46 0.037
350
CLD014 Cole Disease 40 0.037
351
TNC002 Tinea Capitis 38 0.037
352
BLN010 Balanitis 37 0.037
353
DLT018 Dilution, Pigmentary 28 0.037
354
HYP213 Hypomelanotic Disorder 23 0.037
355
c ACQ010 Acquired Polycythemia 46 0.036
356
FCL009 Focal Dermal Hypoplasia 66 0.034
357
HYP001 Hypochromic Microcytic Anemia 38 0.034
358
PLR006 Pleural Cancer 38 0.034
359
EYL002 Eyelid Carcinoma 28 0.034
360
SPL007 Splenic Abscess 28 0.034
361
QNQ002 Quinquaud Folliculitis Decalvans 28 0.034
362
PGT003 Paget Disease, Extramammary 47 0.033
363
OVR105 Ovarian Serous Carcinoma 37 0.033
364
ALC011 Alcoholic Neuropathy 34 0.033
365
INF057 Inflammatory Linear Verrucous Epidermal Nevus 34 0.033
366
c HMC009 Hemochromatosis Type 2 50 0.031
367
P LPC002 Lip Cancer 46 0.031
368
P PRM001 Primary Cutaneous Amyloidosis 44 0.031
369
SWT002 Sweat Gland Cancer 40 0.031
370
TNN002 Tinea Unguium 35 0.031
371
PGM002 Pigmented Basal Cell Carcinoma 32 0.031
372
c BSL011 Basal Cell Carcinoma, Multiple 25 0.031
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