Search results for malnutrition

457 hits were found for malnutrition

# Family MCID Name MIFTS Score
1
PRT038 Protein-Energy Malnutrition 52 7.334
2
NTR005 Nutritional Deficiency Disease 46 3.862
3
KWS001 Kwashiorkor 43 0.208
4
P DRR001 Diarrhea 60 0.194
5
MRS001 Marasmus 39 0.149
6
MLR004 Malaria 86 0.142
7
PRT036 Peritonitis 67 0.142
8
P HPT021 Hepatitis 75 0.135
9
AGN016 Aging 65 0.128
10
P PNC044 Pancreatitis 64 0.120
11
c BLD140 Blood Group, I System 37 0.107
12
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.103
13
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.103
14
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.103
15
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.103
16
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.103
17
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.103
18
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.103
19
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.103
20
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.103
21
XRP001 Xerophthalmia 35 0.103
22
INS024 Insulin-Like Growth Factor I 83 0.098
23
LVR012 Liver Cirrhosis 73 0.098
24
c CHR089 Chronic Kidney Failure 72 0.098
25
P PNM007 Pneumonia 70 0.098
26
P INF038 Influenza 77 0.093
27
P DBT009 Diabetes Mellitus 72 0.093
28
P KDN018 Kidney Disease 69 0.093
29
P THY032 Thyroiditis 56 0.093
30
KRT002 Keratomalacia 55 0.093
31
c BLM008 Bulimia Nervosa 2 53 0.093
32
P INT068 Intestinal Disease 65 0.088
33
MSL001 Measles 64 0.088
34
URM002 Uremia 52 0.088
35
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 33 0.088
36
CYS001 Cystic Fibrosis 85 0.082
37
P LVR013 Liver Disease 76 0.082
38
P LKM002 Leukemia 75 0.082
39
ISC004 Ischemia 66 0.082
40
ACQ007 Acquired Immunodeficiency Syndrome 65 0.082
41
ALC006 Alcoholic Hepatitis 62 0.082
42
GRD001 Giardiasis 45 0.082
43
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.082
44
RCK004 Rickets 63 0.076
45
END030 End Stage Renal Failure 59 0.076
46
IRN001 Iron Deficiency Anemia 55 0.076
47
IRN002 Iron Metabolism Disease 45 0.076
48
P PLL002 Pellagra 44 0.076
49
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.076
50
TRP004 Tropical Sprue 38 0.076
51
P CLR023 Colorectal Cancer 98 0.069
52
P ART022 Arthritis 77 0.069
53
CNG034 Congestive Heart Failure 74 0.069
54
CHY002 Chylomicron Retention Disease 54 0.069
55
OVR063 Overnutrition 53 0.069
56
VSC044 Visceral Myopathy 52 0.069
57
CRY003 Cryptosporidiosis 51 0.069
58
P NGH001 Night Blindness 51 0.069
59
MTB004 Metabolic Acidosis 49 0.069
60
ANC001 Ancylostomiasis 48 0.069
61
DYS073 Dysphagia 47 0.069
62
CRB009 Cerebritis 41 0.069
63
PRT019 Protein-Losing Enteropathy 40 0.069
64
P RHM011 Rheumatoid Arthritis 91 0.062
65
P OST002 Osteoporosis 75 0.062
66
c HPT001 Hepatitis C 73 0.062
67
P MNN013 Meningitis 71 0.062
68
P MYC084 Mycobacterium Tuberculosis 1 69 0.062
69
RSP006 Respiratory System Disease 63 0.062
70
DFC004 Deficiency Anemia 62 0.062
71
MRB003 Morbid Obesity 61 0.062
72
MCS002 Mucositis 61 0.062
73
c ACT073 Acute Leukemia 61 0.062
74
LYS012 Lysosomal Acid Lipase Deficiency 60 0.062
75
URN009 Urinary System Disease 58 0.062
76
CLN019 Colonic Disease 55 0.062
77
P LCT002 Lactose Intolerance 48 0.062
78
DYS015 Dysentery 43 0.062
79
c CNG413 Congenital Short Bowel Syndrome 39 0.062
80
P PNC035 Pancreatic Cancer 89 0.054
81
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.054
82
P NRB001 Neuroblastoma 73 0.054
83
LSH001 Leishmaniasis 71 0.054
84
LNG099 Lung Disease 67 0.054
85
P CLC063 Celiac Disease 1 65 0.054
86
P ESP024 Esophagitis 64 0.054
87
SCH014 Schistosomiasis 62 0.054
88
ETN001 Eating Disorder 61 0.054
89
NTH001 Netherton Syndrome 60 0.054
90
c BCT007 Bacterial Meningitis 59 0.054
91
VSC003 Visceral Leishmaniasis 59 0.054
92
P ENC018 Encephalopathy 58 0.054
93
BRN106 Burns 57 0.054
94
BNF002 Bone Fracture 56 0.054
95
HYP060 Hyperinsulinism 56 0.054
96
P MSC003 Muscular Atrophy 55 0.054
97
FDL002 Food Allergy 55 0.054
98
c MCR113 Microvascular Complications of Diabetes 3 55 0.054
99
SPS003 Spastic Diplegia 55 0.054
100
P INF037 Inflammatory Bowel Disease 52 0.054
101
P SHR001 Short Bowel Syndrome 52 0.054
102
DNT012 Dental Caries 50 0.054
103
HMS001 Hemosiderosis 50 0.054
104
DRR016 Diarrhea 2, with Microvillus Atrophy 48 0.054
105
BRN080 Brain Ischemia 45 0.054
106
c MCR130 Microvascular Complications of Diabetes 6 42 0.054
107
c ACT004 Acute Diarrhea 41 0.054
108
BRB001 Beriberi 40 0.054
109
RCT017 Rectal Disease 38 0.054
110
PSD029 Pseudocholinesterase Deficiency 38 0.054
111
BTN004 Biotin Deficiency 37 0.054
112
c MCR120 Microvascular Complications of Diabetes 7 34 0.054
113
c MCR133 Microvascular Complications of Diabetes 4 32 0.054
114
EXC004 Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis 22 0.054
115
P LNG032 Lung Cancer 99 0.044
116
P HPT023 Hepatocellular Carcinoma 94 0.044
117
CRH001 Crohn's Disease 80 0.044
118
P HRT032 Heart Disease 80 0.044
119
P DLT002 Dilated Cardiomyopathy 76 0.044
120
P NRV007 Nervous System Disease 75 0.044
121
P SCH015 Schizophrenia 71 0.044
122
c JVN010 Juvenile Rheumatoid Arthritis 71 0.044
123
c HPT016 Hepatitis B 68 0.044
124
P ANR048 Aniridia 1 68 0.044
125
DMN002 Dementia 68 0.044
126
SKN016 Skin Disease 68 0.044
127
P LYM026 Lymphoblastic Leukemia 66 0.044
128
GST050 Gastrointestinal System Disease 66 0.044
129
GST045 Gastroenteritis 65 0.044
130
c PRC016 Pre-Eclampsia 65 0.044
131
TTN003 Tetanus 65 0.044
132
APP008 Appendicitis 64 0.044
133
VRL011 Viral Infectious Disease 64 0.044
134
HYP066 Hyperglycemia 64 0.044
135
GNG013 Gingivitis 64 0.044
136
P NRP001 Neuropathy 63 0.044
137
c HPT003 Hepatitis a 63 0.044
138
P ART021 Arteriosclerosis 62 0.044
139
P EXN002 Exanthem 62 0.044
140
TNS005 Tonsillitis 61 0.044
141
P CTR002 Cataract 60 0.044
142
MNT002 Mental Depression 60 0.044
143
c VRL010 Viral Hepatitis 59 0.044
144
PNC034 Pancreas Disease 59 0.044
145
P HYP069 Hyperparathyroidism 58 0.044
146
P MCR010 Microcephaly 57 0.044
147
IMM136 Immune System Disease 57 0.044
148
GST037 Gastroparesis 56 0.044
149
c FRC011 Fructose Intolerance, Hereditary 56 0.044
150
GST009 Gastroschisis 55 0.044
151
BRN071 Brain Injury 54 0.044
152
TBR011 Tuberculous Meningitis 54 0.044
153
LYS003 Lysinuric Protein Intolerance 53 0.044
154
GTR002 Goiter 53 0.044
155
P OBS001 Obstructive Jaundice 53 0.044
156
ALC009 Alcoholic Liver Cirrhosis 53 0.044
157
P PRC012 Pericardial Effusion 52 0.044
158
PRT030 Parathyroid Gland Disease 50 0.044
159
P HYP058 Hypervitaminosis a 48 0.044
160
AMB001 Amebiasis 48 0.044
161
c AMY009 Amyloidosis Aa 48 0.044
162
PLC008 Placenta Disease 48 0.044
163
SKN027 Skin Conditions 48 0.044
164
WRN003 Wernicke Encephalopathy 47 0.044
165
CRD002 Cri-Du-Chat Syndrome 47 0.044
166
GLS007 Glossitis 46 0.044
167
FTL021 Fetal Macrosomia 46 0.044
168
PRS034 Parasitic Helminthiasis Infectious Disease 45 0.044
169
EXC002 Exocrine Pancreatic Insufficiency 45 0.044
170
TRC023 Trichinosis 45 0.044
171
c WLM011 Wilms Tumor 6 44 0.044
172
DNT001 Dental Fluorosis 44 0.044
173
P PRC031 Preeclampsia/eclampsia 1 41 0.044
174
P CRB088 Cerebral Atrophy 38 0.044
175
NCR001 Necrotizing Ulcerative Gingivitis 38 0.044
176
MTC061 Mitochondrial Dna Depletion Syndrome 1 35 0.044
177
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.044
178
VSC049 Visceral Myopathy, Familial, with External Ophthalmoplegia 25 0.044
179
NDD001 Nodding Syndrome 22 0.044
180
MTC055 Mitochondrial Dna Depletion Syndrome 4b 22 0.044
181
HYP727 Hypoglossia with Situs Inversus 16 0.044
182
P MTR062 Maternal Uniparental Disomy of Chromosome 4 15 0.044
183
P ALZ034 Alzheimer Disease 95 0.031
184
c SYS001 Systemic Lupus Erythematosus 86 0.031
185
ALP046 Alport Syndrome, X-Linked 74 0.031
186
SQM006 Squamous Cell Carcinoma 74 0.031
187
MSC157 Muscular Dystrophy, Duchenne Type 74 0.031
188
c HPT073 Hepatitis C Virus 73 0.031
189
SCK003 Sickle Cell Anemia 73 0.031
190
ISC006 Ischemic Heart Disease 73 0.031
191
PLM001 Pulmonary Tuberculosis 72 0.031
192
CHG001 Chagas Disease 72 0.031
193
KWS002 Kawasaki Disease 72 0.031
194
WLS001 Wilson Disease 72 0.031
195
P NSP012 Nasopharyngeal Carcinoma 71 0.031
196
VSC007 Vascular Disease 71 0.031
197
P RSP003 Respiratory Failure 71 0.031
198
P LYM118 Lymphoma 71 0.031
199
P LPS004 Lupus Erythematosus 69 0.031
200
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.031
201
P TRN020 Turner Syndrome 69 0.031
202
P AMY004 Amyloidosis 69 0.031
203
P CRN018 Coronary Artery Anomaly 69 0.031
204
CRB039 Cerebrovascular Disease 68 0.031
205
OBS002 Obsessive-Compulsive Disorder 68 0.031
206
P ADL010 Adult Respiratory Distress Syndrome 67 0.031
207
APN008 Apnea, Obstructive Sleep 67 0.031
208
OTT002 Otitis Media 67 0.031
209
BRN024 Bronchitis 67 0.031
210
CHR066 Chronic Fatigue Syndrome 67 0.031
211
P PRD008 Periodontitis 67 0.031
212
CHD001 Chediak-Higashi Syndrome 67 0.031
213
c SML038 Small Cell Cancer of the Lung 67 0.031
214
TYP007 Typhoid Fever 67 0.031
215
DNG002 Dengue Hemorrhagic Fever 66 0.031
216
P MSC005 Muscular Dystrophy 66 0.031
217
P ENC004 Encephalitis 66 0.031
218
P THL005 Thalassemia 65 0.031
219
P TXP001 Toxoplasmosis 65 0.031
220
P SLP006 Sleep Apnea 65 0.031
221
c CNT035 Central Nervous System Disease 65 0.031
222
RCT015 Reactive Arthritis 65 0.031
223
P CRD224 Cardiofaciocutaneous Syndrome 1 65 0.031
224
OVR029 Ovarian Hyperstimulation Syndrome 64 0.031
225
CHL123 Chlamydia 64 0.031
226
P HRS035 Hirschsprung Disease 1 64 0.031
227
PRD007 Periodontal Disease 64 0.031
228
PMS001 Poems Syndrome 64 0.031
229
MSC152 Muscular Dystrophy, Becker Type 64 0.031
230
KRT001 Keratoconjunctivitis Sicca 63 0.031
231
HMR004 Hemorrhagic Fever with Renal Syndrome 63 0.031
232
P ALC004 Alcohol Abuse 63 0.031
233
IRR002 Irritable Bowel Syndrome 63 0.031
234
P SNS014 Sinusitis 62 0.031
235
BLM001 Bloom Syndrome 62 0.031
236
HYP056 Hypoglycemia 62 0.031
237
FTT001 Fatty Liver Disease 62 0.031
238
HYP266 Hypoxia 61 0.031
239
P CND004 Candidiasis 61 0.031
240
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.031
241
CLF027 Cleft Palate, Isolated 61 0.031
242
P GLL022 Guillain-Barre Syndrome 61 0.031
243
c PNC108 Pancreatitis, Hereditary 60 0.031
244
P PLY014 Polycystic Kidney Disease 60 0.031
245
BLD034 Bile Duct Carcinoma 60 0.031
246
P GST049 Gastrointestinal System Cancer 60 0.031
247
STT001 Status Epilepticus 60 0.031
248
P HMR012 Hemorrhagic Fever 60 0.031
249
P PRT013 Portal Hypertension 59 0.031
250
c HRD002 Hereditary Angioedema 59 0.031
251
HPT019 Hepatic Encephalopathy 59 0.031
252
P FTL001 Fetal Alcohol Syndrome 59 0.031
253
PHR003 Pharyngitis 59 0.031
254
PLC005 Placental Insufficiency 59 0.031
255
LPD008 Lipid Metabolism Disorder 59 0.031
256
ALL026 Allergic Hypersensitivity Disease 59 0.031
257
PLS007 Plasmodium Falciparum Malaria 59 0.031
258
P HYP083 Hypopituitarism 59 0.031
259
FLR002 Filariasis 58 0.031
260
CRM001 Crimean-Congo Hemorrhagic Fever 58 0.031
261
P END033 Endocarditis 58 0.031
262
c MCL062 Mucolipidosis Ii Alpha/beta 58 0.031
263
GLC003 Glucose Intolerance 58 0.031
264
SHG001 Shigellosis 57 0.031
265
c INT072 Intestinal Pseudo-Obstruction 57 0.031
266
P CRN300 Coronary Heart Disease 1 57 0.031
267
P ECL001 Eclampsia 57 0.031
268
P LPD010 Lipodystrophy 57 0.031
269
VND007 Van Der Woude Syndrome 1 57 0.031
270
FCL009 Focal Dermal Hypoplasia 57 0.031
271
P ANG015 Angioedema 57 0.031
272
ECH003 Echinococcosis 57 0.031
273
c HPT007 Hepatitis E 57 0.031
274
EXT034 Extrinsic Allergic Alveolitis 57 0.031
275
P LRY019 Laryngitis 57 0.031
276
CYS005 Cysticercosis 57 0.031
277
P BRN009 Burning Mouth Syndrome 56 0.031
278
CHL014 Cholera 56 0.031
279
P ZLL001 Zellweger Syndrome 56 0.031
280
NNL002 Nonalcoholic Steatohepatitis 56 0.031
281
MST005 Mastitis 56 0.031
282
P PYL005 Pyelonephritis 56 0.031
283
BCT002 Bacterial Vaginosis 56 0.031
284
SLM003 Salmonellosis 56 0.031
285
BLR001 Biliary Atresia 56 0.031
286
PLS006 Plasmodium Vivax Malaria 56 0.031
287
P MYP006 Myopia 56 0.031
288
P HYP076 Hyperthyroidism 56 0.031
289
CRT049 Critical Limb Ischemia 56 0.031
290
DGR001 Digeorge Syndrome 55 0.031
291
PNM001 Pneumocystosis 55 0.031
292
P PMP001 Pemphigus 55 0.031
293
P PNM006 Pneumoconiosis 55 0.031
294
TRY001 Trypanosomiasis 55 0.031
295
P TRC086 Trichohepatoenteric Syndrome 1 54 0.031
296
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.031
297
P RTN022 Retinal Vein Occlusion 53 0.031
298
c VRL007 Viral Encephalitis 53 0.031
299
YLL001 Yellow Nail Syndrome 53 0.031
300
ONC002 Onchocerciasis 53 0.031
301
c CNT075 Central Precocious Puberty 52 0.031
302
TRC008 Trachoma 52 0.031
303
P CHL066 Cholangitis 52 0.031
304
RTN023 Retinitis 52 0.031
305
HPT082 Hepatic Adenomas, Familial 52 0.031
306
c ACT134 Acute Liver Failure 52 0.031
307
ACH005 Achalasia 52 0.031
308
P PRC019 Precocious Puberty 52 0.031
309
MMB001 Membranoproliferative Glomerulonephritis 51 0.031
310
SCH012 Schizoaffective Disorder 51 0.031
311
ART140 Arteries, Anomalies of 51 0.031
312
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 51 0.031
313
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.031
314
P GND004 Gonadal Dysgenesis 50 0.031
315
URC002 Urea Cycle Disorder 50 0.031
316
SCB001 Scabies 50 0.031
317
ELS001 Eales Disease 50 0.031
318
PNC001 Pancytopenia 50 0.031
319
c CNT016 Central Retinal Vein Occlusion 50 0.031
320
MCR191 Microscopic Colitis 50 0.031
321
P TCL004 T-Cell Leukemia 50 0.031
322
MGC001 Megacolon 50 0.031
323
c WLM018 Wilms Tumor 5 49 0.031
324
c EPL169 Epileptic Encephalopathy, Early Infantile, 36 49 0.031
325
BCT004 Bacteriuria 49 0.031
326
MNN009 Meningoencephalitis 49 0.031
327
OCL008 Oculopharyngeal Muscular Dystrophy 49 0.031
328
HYP077 Hypertrichosis 49 0.031
329
MNC006 Monoclonal Gammopathy of Uncertain Significance 49 0.031
330
HYP081 Hypolipoproteinemia 49 0.031
331
P SDR002 Siderosis 48 0.031
332
DWR001 Dwarfism 48 0.031
333
ASC010 Ascaris Lumbricoides Infection 48 0.031
334
P CMP008 Compartment Syndrome 48 0.031
335
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 47 0.031
336
NM001 Noma 46 0.031
337
P DMY001 Demyelinating Polyneuropathy 46 0.031
338
c CRD187 Cardiomyopathy, Dilated, 3b 46 0.031
339
MLK006 Milk Allergy 46 0.031
340
LPD004 Lipoid Nephrosis 46 0.031
341
CHR100 Chronic Ulcer of Skin 46 0.031
342
VTM002 Vitamin B12 Deficiency 46 0.031
343
PRD004 Prediabetes Syndrome 46 0.031
344
END072 Endotheliitis 46 0.031
345
IMP004 Impetigo 45 0.031
346
OBS037 Obesity-Hypoventilation Syndrome 45 0.031
347
CNT025 Central Pontine Myelinolysis 45 0.031
348
IMM154 Immunoglobulin a Deficiency 1 45 0.031
349
P PRT026 Parotitis 45 0.031
350
P ANL018 Analbuminemia 45 0.031
351
FSC002 Fascioliasis 45 0.031
352
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.031
353
DCB001 Decubitus Ulcer 44 0.031
354
P CPL003 Capillary Leak Syndrome 44 0.031
355
VGN020 Vaginal Disease 44 0.031
356
PRL032 Perlman Syndrome 44 0.031
357
TST018 Testicular Yolk Sac Tumor 44 0.031
358
ASP004 Asphyxia Neonatorum 44 0.031
359
TTH032 Tooth Size 44 0.031
360
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 44 0.031
361
MRG013 Mirage Syndrome 44 0.031
362
MCR017 Macrocytic Anemia 44 0.031
363
LYM116 Lymph Node Disease 43 0.031
364
PYM001 Pyomyositis 42 0.031
365
MCR020 Microsporidiosis 42 0.031
366
SPR007 Superior Mesenteric Artery Syndrome 42 0.031
367
STT004 Steatorrhea 41 0.031
368
FRM003 Farmer's Lung 41 0.031
369
AMN006 Aminoaciduria 41 0.031
370
c CRN278 Craniosynostosis 1 41 0.031
371
OST097 Osteoporotic Fracture 41 0.031
372
TNS007 Taeniasis 41 0.031
373
c ADL027 Adult Dermatomyositis 41 0.031
374
SNL007 Senile Cataract 41 0.031
375
P HVY001 Heavy Chain Disease 41 0.031
376
ANR018 Anorchia 40 0.031
377
STR077 Streptococcal Toxic-Shock Syndrome 40 0.031
378
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.031
379
HPT004 Hepatic Coma 40 0.031
380
ETH004 Euthyroid Sick Syndrome 40 0.031
381
C1N001 C1 Inhibitor Deficiency 40 0.031
382
TRC077 Trichomegaly 40 0.031
383
c CHR096 Chronic Pulmonary Heart Disease 39 0.031
384
MLN003 Melancholia 39 0.031
385
MLT002 Multiple Symmetrical Lipomatosis 39 0.031
386
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.031
387
GLC008 Glucose Metabolism Disease 38 0.031
388
OST008 Osteosclerotic Myeloma 38 0.031
389
RTC003 Root Caries 38 0.031
390
ALC010 Alcoholic Cardiomyopathy 38 0.031
391
ECT004 Ecthyma 38 0.031
392
c RTN069 Retinitis Pigmentosa 7 38 0.031
393
CHL039 Choledocholithiasis 38 0.031
394
PST010 Pasteurellosis 37 0.031
395
CHY005 Chylothorax, Congenital 37 0.031
396
HPT008 Hepatic Tuberculosis 37 0.031
397
PYR016 Pyridoxine Deficiency 37 0.031
398
IMM003 Immunoglobulin Alpha Deficiency 37 0.031
399
P ART106 Arterial Calcification, Generalized, of Infancy, 1 36 0.031
400
BLP001 Blepharochalasis 36 0.031
401
TTH007 Tooth Erosion 36 0.031
402
c HYP072 Hypersensitivity Reaction Type Iii Disease 35 0.031
403
MSC012 Muscular Dystrophy, Duchenne and Becker Type 35 0.031
404
P FML187 Familial Hypertension 35 0.031
405
ACR005 Acrodermatitis 35 0.031
406
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 35 0.031
407
HYP001 Hypochromic Microcytic Anemia 34 0.031
408
PYR004 Pyuria 34 0.031
409
PLY010 Polyclonal Hypergammaglobulinemia 34 0.031
410
RFR013 Refractory Celiac Disease 34 0.031
411
NSP003 Nasopharyngeal Disease 34 0.031
412
HMP001 Hemopericardium 34 0.031
413
MCL069 Macular Dystrophy, Retinal, 1, North Carolina Type 34 0.031
414
c DNR003 Duane Retraction Syndrome 1 34 0.031
415
SCR037 Sucrase-Isomaltase Deficiency, Congenital 33 0.031
416
SCR039 Scorpion Envenomation 33 0.031
417
GRW036 Growth Control, Y-Chromosome Influenced 33 0.031
418
c RTN090 Retinitis Pigmentosa 55 33 0.031
419
ALT002 Aleutian Mink Disease 33 0.031
420
BRL001 Brill-Zinsser Disease 33 0.031
421
TMP011 Temple-Baraitser Syndrome 32 0.031
422
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.031
423
P ACQ009 Acquired Metabolic Disease 32 0.031
424
c MYT029 Myotonia Congenita, Autosomal Recessive 32 0.031
425
P KLZ004 Kala-Azar 1 31 0.031
426
AMY002 Amyloid Tumor 30 0.031
427
ALR002 Al-Raqad Syndrome 30 0.031
428
ATR073 Atrophic Glossitis 30 0.031
429
NLL001 Null-Cell Leukemia 29 0.031
430
PMP008 Pemphigus Vegetans 29 0.031
431
P PLT008 Pili Torti 29 0.031
432
ORT001 Orthostatic Proteinuria 29 0.031
433
MDN001 Median Rhomboid Glossitis 28 0.031
434
P STR035 Streptococcal Group a Invasive Disease 28 0.031
435
HYP029 Hyperthyroxinemia 27 0.031
436
OSM001 Osmotic Diarrhea 27 0.031
437
c ALP087 Alpha-Heavy Chain Disease 27 0.031
438
CRT011 Carotenemia 26 0.031
439
MNN024 Meningitis and Encephalitis 26 0.031
440
5XP001 5-Oxoprolinase Deficiency 25 0.031
441
HNM002 Hinman Syndrome 25 0.031
442
CMM006 Commensal Bacterial Infectious Disease 24 0.031
443
BLD163 Blood Group, Dombrock System 23 0.031
444
CRK001 Cork-Handlers' Disease 22 0.031
445
HYP481 Hyperbiliverdinemia 22 0.031
446
ANR038 Anorexia Nervosa 1 21 0.031
447
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.031
448
c DRM055 Dermatitis, Atopic, 3 21 0.031
449
OST007 Ostertagiasis 20 0.031
450
OGL001 Ogilvie Syndrome 20 0.031
451
c HYP290 Hypobetalipoproteinemia, Familial, 2 18 0.031
452
PRM123 Paramyloidosis 18 0.031
453
BLD137 Blood Group--Ahonen 17 0.031
454
c CLC037 Celiac Disease 4 16 0.031
455
c CLC048 Celiac Disease 3 16 0.031
456
ULC003 Ulcerative Blepharitis 15 0.031
457
c CLC039 Celiac Disease 13 15 0.031
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