Search results for Adenosine monophosphate

422 hits were found for Adenosine monophosphate

# Family MCID Name MIFTS Score
1
ADN029 Adenosine Monophosphate Deaminase 1 Deficiency 34 6.982
2
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 27 4.352
3
ERY039 Erythrocyte Amp Deaminase Deficiency 19 3.072
4
ISC004 Ischemia 67 0.248
5
AST005 Asthma 81 0.198
6
P LKM002 Leukemia 72 0.194
7
P OVR042 Ovarian Cancer 83 0.189
8
MYL069 Myeloma, Multiple 85 0.186
9
BRR014 Barrett Esophagus 70 0.177
10
HYP266 Hypoxia 63 0.173
11
BRK010 Burkitt Lymphoma 69 0.173
13
P HPT021 Hepatitis 73 0.154
14
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.147
15
P MNN013 Meningitis 69 0.141
16
P ADN016 Adenocarcinoma 70 0.135
17
P BRS047 Breast Cancer 100 0.131
18
P RHM011 Rheumatoid Arthritis 81 0.126
19
P RTN008 Retinitis Pigmentosa 80 0.123
20
P DBT005 Diabetes Insipidus 55 0.122
21
P LYM118 Lymphoma 69 0.120
22
P DBT009 Diabetes Mellitus 67 0.119
23
P LYM031 Lymphocytic Leukemia 61 0.119
24
CNG034 Congestive Heart Failure 70 0.118
25
WLF001 Wolff-Parkinson-White Syndrome 61 0.118
26
P MYC007 Myocardial Infarction 78 0.118
27
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 30 0.117
28
CHR074 Choriocarcinoma 49 0.117
29
P LVR013 Liver Disease 76 0.116
30
P PRS040 Prostate Cancer 93 0.116
31
P ART022 Arthritis 77 0.116
32
P NRP001 Neuropathy 63 0.115
33
ESP021 Esophageal Cancer 82 0.112
34
c HYP595 Hypertension, Essential 81 0.112
35
P PLM037 Pulmonary Hypertension 77 0.112
36
c PRS136 Prostate Cancer, Hereditary, 6 40 0.109
37
c PRS130 Prostate Cancer, Hereditary, 8 37 0.109
38
HMT018 Hematopoietic Stem Cell Transplantation 59 0.109
39
SPN012 Spindle Cell Hemangioma 36 0.106
40
INS024 Insulin-Like Growth Factor I 82 0.105
41
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.104
42
P HML002 Hemolytic Anemia 64 0.102
43
MST004 Mast Cell Neoplasm 42 0.101
44
EXT007 Extracutaneous Mastocytoma 41 0.101
45
CYS001 Cystic Fibrosis 82 0.100
46
c LKM061 Leukemia, Acute Myeloid 81 0.100
47
ADR054 Adrenocortical Carcinoma, Hereditary 59 0.098
48
ADR016 Adrenal Cortical Carcinoma 57 0.098
49
ADR004 Adrenal Cortical Adenocarcinoma 48 0.098
50
c SYS001 Systemic Lupus Erythematosus 88 0.097
51
P LPS004 Lupus Erythematosus 69 0.097
52
NTR027 Neutrophil Actin Dysfunction 32 0.097
53
c LKM071 Leukemia, Chronic Lymphocytic 78 0.096
54
P ATR011 Atrial Fibrillation 69 0.096
55
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.095
56
P GRF003 Graft-Versus-Host Disease 71 0.094
57
P CLR023 Colorectal Cancer 99 0.094
58
c AMY091 Amyotrophic Lateral Sclerosis 1 90 0.094
59
P MYL006 Myeloid Leukemia 67 0.093
60
INT002 Intermittent Claudication 64 0.093
61
c ACT210 Acute Respiratory Distress Syndrome 66 0.092
62
P MSC007 Muscle Hypertrophy 64 0.092
63
c LKM004 Leukemia, B-Cell, Chronic 38 0.091
64
DPR016 Depression 72 0.091
65
P LNG032 Lung Cancer 99 0.090
66
c HPT016 Hepatitis B 70 0.090
67
GST053 Gastric Cancer 78 0.089
68
IMM136 Immune System Disease 57 0.089
69
MLN008 Melanoma 63 0.089
70
DBT010 Diabetic Neuropathy 60 0.088
71
P HPT023 Hepatocellular Carcinoma 96 0.087
72
P LYM033 Lymphoproliferative Syndrome 63 0.086
73
P PSD015 Pseudohypoparathyroidism 51 0.086
74
BNR002 Bone Resorption Disease 54 0.085
75
CHL014 Cholera 60 0.084
76
P LTR001 Lateral Sclerosis 60 0.084
77
LVR012 Liver Cirrhosis 67 0.083
78
P HYP073 Hypersensitivity Reaction Type Iv Disease 50 0.082
79
GST033 Gestational Diabetes 63 0.081
80
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 67 0.081
81
THR024 Thrombosis 64 0.080
82
HML018 Homologous Wasting Disease 24 0.079
83
c MCR113 Microvascular Complications of Diabetes 3 58 0.078
84
c MCR120 Microvascular Complications of Diabetes 7 46 0.078
85
c MCR130 Microvascular Complications of Diabetes 6 43 0.078
86
c MCR133 Microvascular Complications of Diabetes 4 43 0.078
87
P AST007 Astrocytoma 52 0.078
88
LYM133 Lymphoma, Hodgkin, Classic 72 0.078
89
LYM019 Lymphosarcoma 53 0.078
90
CLT003 Colitis 65 0.078
91
P GLM045 Glioma 55 0.078
92
GLB002 Glioblastoma 74 0.076
93
P SCH015 Schizophrenia 73 0.076
94
P CRD119 Cardiac Arrest 66 0.076
95
MLR004 Malaria 84 0.076
96
THY028 Thyroid Cancer 72 0.076
97
SCK005 Sickle Cell Disease 57 0.076
98
PTT037 Pituitary Tumors 48 0.076
99
c FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.075
100
P ALZ034 Alzheimer Disease 87 0.074
101
c ACT074 Acute Lymphocytic Leukemia 63 0.074
102
IMP005 Impotence 56 0.074
103
P KDN018 Kidney Disease 71 0.073
104
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.073
105
RSP006 Respiratory System Disease 64 0.073
106
PRT037 Pertussis 70 0.072
107
ACH004 Achondroplasia 68 0.072
108
IGR001 Ige Responsiveness, Atopic 59 0.072
109
LYM024 Lymphatic System Disease 54 0.072
110
HYP066 Hyperglycemia 64 0.071
111
TRN015 Transient Cerebral Ischemia 59 0.071
112
HPR003 Heparin-Induced Thrombocytopenia 53 0.071
113
P PNM007 Pneumonia 72 0.070
114
SCK003 Sickle Cell Anemia 74 0.070
115
P DRM053 Dermatitis, Atopic 71 0.070
116
ALL003 Allergic Rhinitis 70 0.070
117
DRM006 Dermatitis 69 0.070
118
P MJR001 Major Depressive Disorder 67 0.070
119
OST159 Osteogenic Sarcoma 66 0.070
120
P RHN004 Rhinitis 64 0.070
121
URM002 Uremia 53 0.070
122
MYL009 Myelodysplastic Syndrome 70 0.069
123
P LKM062 Leukemia, Acute Lymphoblastic 68 0.069
124
MYL031 Myeloproliferative Neoplasm 64 0.069
125
LYM067 Lymphoid Leukemia 47 0.069
126
BLD054 Blood Protein Disease 43 0.069
127
ACT118 Acute Non Lymphoblastic Leukemia 32 0.069
128
c ATR087 Atrial Standstill 1 70 0.068
129
ALL026 Allergic Hypersensitivity Disease 68 0.068
130
BRN002 Bronchiolitis 61 0.068
131
P TRC086 Trichohepatoenteric Syndrome 1 60 0.068
132
BRN012 Bronchiolitis Obliterans 59 0.068
133
THR013 Thoracic Outlet Syndrome 56 0.068
134
ADN018 Adenoma 64 0.066
135
c CNG027 Congenital Hemolytic Anemia 53 0.066
136
ALL014 Allergic Encephalomyelitis 43 0.066
137
HMN044 Human Immunodeficiency Virus Type 1 75 0.066
138
MVM001 Movement Disease 67 0.066
139
ALL006 Allergic Asthma 61 0.066
140
c HPT073 Hepatitis C Virus 72 0.064
141
VRL011 Viral Infectious Disease 68 0.064
142
DPH001 Diphtheria 63 0.064
143
P HMR003 Hemorrhagic Disease 59 0.064
144
LYM040 Lymphoblastic Lymphoma 57 0.064
145
P HYP024 Hypoparathyroidism 55 0.064
146
P BLD051 Blood Coagulation Disease 52 0.064
147
VSC008 Vascular Hemostatic Disease 43 0.064
148
P PHC003 Pheochromocytoma 72 0.064
149
c LKM056 Leukemia, Chronic Lymphocytic 2 43 0.064
150
c HPT001 Hepatitis C 69 0.064
151
c CHR417 Chronic Graft Versus Host Disease 66 0.064
152
c LKM063 Leukemia, Chronic Myeloid 73 0.063
153
HMG005 Hemoglobinopathy 54 0.063
154
P FML068 Familial Hypocalciuric Hypercalcemia 50 0.063
155
PMP004 Pemphigus Foliaceus 46 0.063
156
TRT001 Teratocarcinoma 41 0.063
157
SRC014 Sarcoma 70 0.063
158
FTT001 Fatty Liver Disease 66 0.063
159
HYP056 Hypoglycemia 64 0.063
160
LSC001 Lesch-Nyhan Syndrome 62 0.063
161
P HYP061 Hypertrophic Cardiomyopathy 59 0.063
162
URT010 Ureteral Obstruction 49 0.063
163
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 44 0.063
164
P MLT020 Multiple Sclerosis 75 0.062
165
c PLM164 Pulmonary Hypertension, Primary, 1 70 0.062
166
P MLG056 Malignant Hyperthermia 60 0.062
167
SQM006 Squamous Cell Carcinoma 58 0.062
168
P TCL004 T-Cell Leukemia 53 0.062
169
P BLD134 Bladder Cancer 70 0.059
170
ANR007 Anorexia Nervosa 68 0.059
171
P ANR048 Aniridia 1 64 0.059
172
ACN002 Acanthosis Nigricans 64 0.059
173
P GRV001 Graves' Disease 61 0.059
174
P INF037 Inflammatory Bowel Disease 56 0.059
175
RNL077 Renal Fibrosis 51 0.059
176
FSH001 Fish-Eye Disease 50 0.059
177
ATX010 Ataxia Neuropathy Spectrum 39 0.059
178
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 38 0.059
179
PPL052 Papillomatosis, Confluent and Reticulated 33 0.059
180
P ACT232 Acute Necrotizing Encephalopathy 30 0.059
181
BLD137 Blood Group--Ahonen 24 0.059
182
P MCR115 Microvascular Complications of Diabetes 5 70 0.059
183
c SML038 Small Cell Cancer of the Lung 68 0.059
184
P PRP019 Peripheral Nervous System Disease 66 0.059
185
GLB015 Glioblastoma Multiforme 64 0.059
186
AGN016 Aging 63 0.059
187
HDC001 Headache 62 0.059
188
P NTR004 Neutropenia 60 0.059
189
BRN080 Brain Ischemia 43 0.059
190
c ACT135 Acute Graft Versus Host Disease 58 0.058
191
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 29 0.058
192
c VRL010 Viral Hepatitis 60 0.058
193
P CYS018 Cystitis 58 0.058
194
P RCT021 Rectum Cancer 58 0.058
195
ATM095 Autoimmune Disease 68 0.056
196
P ENC018 Encephalopathy 65 0.056
197
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.056
198
c BCT007 Bacterial Meningitis 61 0.056
199
STT001 Status Epilepticus 60 0.056
200
GST023 Gastric Ulcer 58 0.056
201
GST071 Gastrointestinal Carcinoma 45 0.056
202
6PH001 6-Phosphogluconate Dehydrogenase Deficiency 29 0.056
203
P PNC035 Pancreatic Cancer 82 0.056
204
P INF038 Influenza 75 0.056
205
c WLM018 Wilms Tumor 5 64 0.056
206
PST028 Post-Traumatic Stress Disorder 63 0.056
207
P OST001 Osteopetrosis 63 0.056
208
P GLM007 Glomerulonephritis 61 0.056
209
c PRM005 Primary Hyperparathyroidism 60 0.056
210
P HYP069 Hyperparathyroidism 59 0.056
211
P NNL004 Nonalcoholic Fatty Liver Disease 56 0.056
212
ATN002 Autonomic Nervous System Disease 56 0.056
213
NSD001 Nose Disease 52 0.056
214
RSP021 Respiratory Allergy 48 0.056
215
P DYS021 Dysautonomia 45 0.056
216
OST012 Osteoarthritis 80 0.053
217
ULC004 Ulcerative Colitis 80 0.053
218
P NRV007 Nervous System Disease 71 0.053
219
THR100 Thrombocytopenic Purpura, Autoimmune 67 0.053
220
DFC004 Deficiency Anemia 66 0.053
221
P VSC011 Vasculitis 66 0.053
222
GST049 Gastrointestinal System Cancer 62 0.053
223
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 62 0.053
224
P BPL003 Bipolar Disorder 61 0.053
225
P PNS012 Paine Syndrome 60 0.053
226
OVR094 Ovarian Epithelial Cancer 41 0.053
227
P GLY013 Glycogen Storage Disease 61 0.052
228
MCS002 Mucositis 60 0.052
229
TXC002 Toxic Encephalopathy 57 0.052
230
CPL005 Capillary Disease 45 0.052
231
LYM143 Lymphoma, Non-Hodgkin, Familial 73 0.051
232
c ATM011 Autoimmune Hepatitis 67 0.051
233
CLF027 Cleft Palate, Isolated 64 0.051
234
c ACT073 Acute Leukemia 62 0.051
235
CLN015 Colon Adenocarcinoma 57 0.051
236
c GRV008 Graves Disease 1 57 0.051
237
GTR002 Goiter 54 0.051
238
PRT029 Parathyroid Adenoma 52 0.051
239
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 49 0.051
240
BSL008 Basal Ganglia Disease 48 0.051
241
c WLM011 Wilms Tumor 6 40 0.051
242
CRV035 Cervical Cancer 76 0.050
243
MYC006 Mycosis Fungoides 73 0.050
244
P CHR012 Chronic Granulomatous Disease 69 0.050
245
c MCR129 Microvascular Complications of Diabetes 1 66 0.050
246
P ENC004 Encephalitis 66 0.050
247
NRF007 Neurofibroma 66 0.050
248
P END044 Endometriosis 65 0.050
249
MDD011 Mood Disorder 65 0.050
250
P PLY014 Polycystic Kidney Disease 62 0.050
251
NRM005 Neuromuscular Disease 61 0.050
252
P CHN012 Chondrosarcoma 56 0.050
253
P HYP076 Hyperthyroidism 55 0.050
254
CLR109 Colorectal Adenocarcinoma 54 0.050
255
P NRB010 Neuroblastoma 1 51 0.050
256
PST053 Postherpetic Neuralgia 45 0.050
257
HPT004 Hepatic Coma 45 0.050
258
c MCR112 Microvascular Complications of Diabetes 2 42 0.050
259
SQM013 Squamous Cell Carcinoma, Head and Neck 82 0.046
260
P HRP006 Herpes Simplex 71 0.046
261
P AGM001 Agammaglobulinemia 71 0.046
262
P DMN001 Diamond-Blackfan Anemia 70 0.046
263
MYL005 Myelofibrosis 69 0.046
264
PNC033 Pancreas Adenocarcinoma 67 0.046
265
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.046
266
MNT002 Mental Depression 65 0.046
267
PRT058 Pure Autonomic Failure 65 0.046
268
PPT005 Peptic Ulcer Disease 63 0.046
269
P PNC044 Pancreatitis 62 0.046
270
AND002 Androgen Insensitivity Syndrome 61 0.046
271
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.046
272
c ACT027 Acute Pancreatitis 59 0.046
273
DSS009 Disseminated Intravascular Coagulation 58 0.046
274
P AXN002 Axenfeld-Rieger Syndrome 57 0.046
275
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.046
276
PRP016 Paraplegia 54 0.046
277
NNL002 Nonalcoholic Steatohepatitis 54 0.046
278
c DMN023 Diamond-Blackfan Anemia 1 53 0.046
279
P THY032 Thyroiditis 53 0.046
280
P RNV001 Renovascular Hypertension 52 0.046
281
KRT002 Keratomalacia 51 0.046
282
HMP009 Haemophilus Influenzae 51 0.046
283
MTB004 Metabolic Acidosis 50 0.046
284
MLG086 Malignant Hyperthermia Susceptibility 41 0.046
285
ALR002 Al-Raqad Syndrome 40 0.046
286
P NPH012 Nephrotic Syndrome 63 0.045
287
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.045
288
HDG004 Hodgkin's Granuloma 30 0.045
289
HDG006 Hodgkin's Paragranuloma 22 0.045
290
PFF001 Pfeiffer Syndrome 80 0.042
291
PSY004 Psychotic Disorder 74 0.042
292
ADR007 Adrenoleukodystrophy 71 0.042
293
CNN003 Conn's Syndrome 70 0.042
294
c WLM013 Wilms Tumor 1 68 0.042
295
P FLL037 Follicular Lymphoma 67 0.042
296
HSH003 Hashimoto Thyroiditis 67 0.042
297
LGH007 Leigh Syndrome 67 0.042
298
GST040 Gastric Adenocarcinoma 66 0.042
299
LPD008 Lipid Metabolism Disorder 65 0.042
300
P SNS014 Sinusitis 65 0.042
301
BND020 Bone Disease 64 0.042
302
P MYP004 Myopathy 64 0.042
303
JNT002 Joint Disorders 64 0.042
304
c LRG017 Large Intestine Cancer 63 0.042
305
CLN019 Colonic Disease 62 0.042
306
P INT068 Intestinal Disease 62 0.042
307
PLS011 Plasmacytoma 62 0.042
308
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 0.042
309
P PRT013 Portal Hypertension 61 0.042
310
BRN056 Bronchopulmonary Dysplasia 60 0.042
311
P INF032 Infertility 60 0.042
312
PLM010 Pulmonary Edema 59 0.042
313
PTT009 Pituitary Gland Disease 59 0.042
314
PNC034 Pancreas Disease 59 0.042
315
BRN004 Brain Edema 59 0.042
316
INT253 Intestinal Benign Neoplasm 57 0.042
317
P RTN016 Retinal Degeneration 56 0.042
318
P PTT006 Pituitary Adenoma 54 0.042
319
AMN003 Amnestic Disorder 53 0.042
320
c HPT015 Hepatitis D 52 0.042
321
P PRR002 Pure Red-Cell Aplasia 52 0.042
322
IDP024 Idiopathic Inflammatory Myopathy 52 0.042
323
c PNC106 Pancreatic Agenesis 1 51 0.042
324
OCL069 Ocular Motor Apraxia 49 0.042
325
DNG001 Dengue Shock Syndrome 48 0.042
326
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 46 0.042
327
SLT001 Solitary Osseous Plasmacytoma 44 0.042
328
ADR022 Adrenomyeloneuropathy 43 0.042
329
RCT017 Rectal Disease 43 0.042
330
MRP001 Morphine Dependence 42 0.042
331
ATM052 Autoimmune Disease 1 40 0.042
332
c PCH010 Pachyonychia Congenita 3 40 0.042
333
CRB079 Cerebrospinal Fluid Leak 38 0.042
334
MYT011 Myotonia 34 0.042
335
PRN021 Paranasal Sinus Disease 32 0.042
336
BLD163 Blood Group, Dombrock System 27 0.042
338
P RSP003 Respiratory Failure 72 0.036
339
c THR092 Thrombophilia Due to Thrombin Defect 69 0.036
340
P HYP098 Hypereosinophilic Syndrome 67 0.036
341
RCK004 Rickets 66 0.036
342
LPD016 Lipoid Proteinosis of Urbach and Wiethe 66 0.036
343
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 66 0.036
344
MCC012 Mccune-Albright Syndrome 65 0.036
345
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 0.036
346
CLR108 Colorectal Adenoma 64 0.036
347
INC002 Inclusion Body Myositis 63 0.036
348
P FTL001 Fetal Alcohol Syndrome 63 0.036
349
P BNC003 Bone Cancer 62 0.036
350
FCT002 Factor Xi Deficiency 62 0.036
351
P BRG001 Brugada Syndrome 61 0.036
352
HPT019 Hepatic Encephalopathy 60 0.036
353
END041 Endometrial Adenocarcinoma 60 0.036
354
THY121 Thyroid Gland Anaplastic Carcinoma 59 0.036
355
ACT119 Acute Promyelocytic Leukemia 59 0.036
356
P CTR002 Cataract 59 0.036
357
c MCP004 Mucopolysaccharidosis Iv 59 0.036
358
c PRT132 Protoporphyria, Erythropoietic, 1 58 0.036
359
P PLY041 Polymyositis 58 0.036
360
PTT046 Pituitary Hormone Deficiency, Combined, 2 56 0.036
361
c GLY004 Glycogen Storage Disease V 56 0.036
362
P PMP001 Pemphigus 56 0.036
363
P MSC003 Muscular Atrophy 56 0.036
364
CYS039 Cystic Kidney Disease 55 0.036
365
PLY023 Polycystic Liver Disease 55 0.036
366
P LMB006 Limb-Girdle Muscular Dystrophy 55 0.036
367
P END047 Endophthalmitis 54 0.036
368
MYL004 Myelodysplastic Myeloproliferative Cancer 54 0.036
369
ATY042 Atypical Chronic Myeloid Leukemia 53 0.036
370
P MTC069 Mitochondrial Disorders 53 0.036
371
GNG002 Ganglioneuroma 53 0.036
372
GNG005 Gangliocytoma 52 0.036
373
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 52 0.036
374
ALC009 Alcoholic Liver Cirrhosis 52 0.036
375
LKC003 Leukocyte Disease 52 0.036
376
P MTC133 Mitochondrial Myopathy 52 0.036
377
GRN017 Granulocytopenia 51 0.036
378
ISL001 Islet Cell Tumor 51 0.036
379
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 50 0.036
380
P RNL017 Renal Oncocytoma 50 0.036
381
CNG028 Congenital Hypoplastic Anemia 50 0.036
382
P MYT023 Myotonia Congenita 49 0.036
383
RNL011 Renal Osteodystrophy 49 0.036
384
ACT017 Acute Chest Syndrome 48 0.036
385
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.036
386
IDP073 Idiopathic Hypercalciuria 48 0.036
387
OCL052 Ocular Dominance 48 0.036
388
P OLV001 Olivopontocerebellar Atrophy 48 0.036
389
SGW002 Segawa Syndrome, Autosomal Recessive 48 0.036
390
ANC002 Anca-Associated Vasculitis 47 0.036
391
DWR001 Dwarfism 47 0.036
392
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.036
393
NDL007 Nodular Goiter 47 0.036
394
P END039 Endodermal Sinus Tumor 47 0.036
395
SKL017 Skeletal Dysplasias 46 0.036
396
c ATS282 Autosomal Recessive Malignant Osteopetrosis 46 0.036
397
P HYP263 Hypersomnia 45 0.036
398
P MND003 Mandibuloacral Dysplasia with Type a Lipodystrophy 44 0.036
399
MYX004 Myxedema 43 0.036
400
P HYP265 Hypotonia 43 0.036
401
BWN003 Bowenoid Papulosis 42 0.036
402
HYP026 Hypoglycemic Coma 42 0.036
404
IDP033 Idiopathic Edema 41 0.036
405
FML063 Familial Glucocorticoid Deficiency 41 0.036
406
SNL007 Senile Cataract 40 0.036
407
ADN022 Adenylosuccinase Deficiency 40 0.036
408
ACR002 Acrocapitofemoral Dysplasia 39 0.036
409
MYP001 Myoepithelioma 39 0.036
410
P THP004 Thiopurines, Poor Metabolism of, 1 38 0.036
411
GGN002 Gigantism 36 0.036
412
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 35 0.036
413
c PSD104 Pseudohypoparathyroidism, Type Ii 34 0.036
414
P MRQ003 Morquio Syndrome 33 0.036
415
c EPS039 Episodic Pain Syndrome, Familial, 1 31 0.036
416
PTT001 Pituitary Hypoplasia 29 0.036
417
c PRS080 Prostate Cancer, Hereditary, 7 28 0.036
418
BLD151 Blood Group--Wright Antigen 26 0.036
419
CHR158 Charles Bonnet Syndrome 26 0.036
420
BLD153 Blood Group--Swann System 25 0.036
421
ACT096 Acute Cholinergic Dysautonomia 19 0.036
422
NCL008 Nuclear Ribonucleic Acid 15 0.036
Content
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