Search results for "malnutrition"

The MalaCard for "malnutrition" has been retired.
Searching MalaCards for entries containing "malnutrition"

484 hits were found for 'malnutrition'

# Family MCID Name MIFTS Score
1
PRT038 Protein-Energy Malnutrition 49 7.275
2
NTR005 Nutritional Deficiency Disease 39 3.261
3
KWS001 Kwashiorkor 44 0.200
4
P DRR001 Diarrhea 51 0.175
5
MRS001 Marasmus 39 0.144
6
PRT036 Peritonitis 62 0.138
7
MLR004 Malaria 79 0.135
8
P HPT021 Hepatitis 70 0.131
9
c ACT004 Acute Diarrhea 38 0.128
10
P PNC044 Pancreatitis 60 0.116
11
ACD009 Acid-Labile Subunit, Deficiency of 48 0.104
12
P OBS005 Obesity 93 0.100
13
ATH003 Atherosclerosis 62 0.100
14
XRP001 Xerophthalmia 35 0.100
15
c DRR009 Diarrhea 6 31 0.100
16
DFC004 Deficiency Anemia 65 0.095
17
ETN001 Eating Disorder 60 0.095
18
INS024 Insulin-Like Growth Factor I 74 0.090
19
LVR012 Liver Cirrhosis 67 0.090
20
P PNM007 Pneumonia 66 0.090
21
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.090
22
P ANR007 Anorexia Nervosa 63 0.090
23
P THY032 Thyroiditis 54 0.090
24
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.090
25
MSL001 Measles 61 0.085
26
ASC002 Ascariasis 38 0.085
27
CYS001 Cystic Fibrosis 86 0.080
28
P RCK004 Rickets 59 0.080
29
ALC006 Alcoholic Hepatitis 59 0.080
30
ISC004 Ischemia 59 0.080
31
URM002 Uremia 50 0.080
32
LPD004 Lipoid Nephrosis 48 0.080
33
GRD001 Giardiasis 40 0.080
34
P INF038 Influenza 74 0.074
35
P LVR013 Liver Disease 72 0.074
36
P LKM002 Leukemia 70 0.074
37
TBR010 Tuberculosis 69 0.074
38
c CHR089 Chronic Kidney Failure 66 0.074
39
ADM013 Adamantinoma of Long Bones 59 0.074
40
IRN001 Iron Deficiency Anemia 51 0.074
41
P PLL002 Pellagra 45 0.074
42
MSC004 Muscle Tissue Disease 36 0.074
43
TRP004 Tropical Sprue 36 0.074
44
P CLR023 Colorectal Cancer 97 0.067
45
P ART022 Arthritis 75 0.067
46
FDL002 Food Allergy 54 0.067
47
KRT002 Keratomalacia 54 0.067
48
END030 End Stage Renal Failure 52 0.067
49
P NGH001 Night Blindness 49 0.067
50
DYS073 Dysphagia 49 0.067
51
MTB004 Metabolic Acidosis 48 0.067
52
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.067
53
SPC010 Speech and Communication Disorders 46 0.067
54
PRT019 Protein-Losing Enteropathy 41 0.067
55
CRB009 Cerebritis 38 0.067
56
BNS002 Bone Structure Disease 36 0.067
57
P RHM011 Rheumatoid Arthritis 88 0.060
58
CNG034 Congestive Heart Failure 71 0.060
59
c HPT001 Hepatitis C 68 0.060
60
P MYP004 Myopathy 67 0.060
61
c ACT073 Acute Leukemia 62 0.060
62
P INT068 Intestinal Disease 61 0.060
63
P GST049 Gastrointestinal System Cancer 60 0.060
64
CHY002 Chylomicron Retention Disease 59 0.060
65
MRB003 Morbid Obesity 58 0.060
66
P MSC033 Muscle Disorders 52 0.060
67
LRN003 Learning Disability 51 0.060
68
CLN019 Colonic Disease 50 0.060
69
INT253 Intestinal Benign Neoplasm 50 0.060
70
CRY003 Cryptosporidiosis 46 0.060
71
LCT002 Lactose Intolerance 45 0.060
72
BRN080 Brain Ischemia 41 0.060
73
BLD054 Blood Protein Disease 40 0.060
74
FNC002 Functional Diarrhea 38 0.060
75
IMP003 Impaired Renal Function Disease 37 0.060
76
c DRR007 Diarrhea 7 33 0.060
77
BNM008 Bone Mineral Density, Low 19 0.060
78
HPT023 Hepatocellular Carcinoma 91 0.052
79
P PNC035 Pancreatic Cancer 85 0.052
80
P NRB001 Neuroblastoma 69 0.052
81
P CRD011 Cardiomyopathy 67 0.052
82
P CLC005 Celiac Disease 67 0.052
83
P MNN013 Meningitis 65 0.052
84
P OST002 Osteoporosis 64 0.052
85
LNG099 Lung Disease 62 0.052
86
LSH001 Leishmaniasis 62 0.052
87
P ESP024 Esophagitis 62 0.052
88
c VRL010 Viral Hepatitis 61 0.052
89
P HYP060 Hyperinsulinism 59 0.052
90
PNC034 Pancreas Disease 57 0.052
91
VSC003 Visceral Leishmaniasis 55 0.052
92
RCT018 Rectal Neoplasm 55 0.052
93
URN009 Urinary System Disease 53 0.052
94
P SPS003 Spastic Diplegia 53 0.052
95
BRN071 Brain Injury 52 0.052
96
P URF003 Urofacial Syndrome 1 52 0.052
97
BRN106 Burns 52 0.052
98
VSC044 Visceral Myopathy 51 0.052
99
STM006 Stomach Disease 50 0.052
100
HYP037 Hyperhomocysteinemia 50 0.052
101
OVR063 Overnutrition 49 0.052
102
CSY001 C Syndrome 49 0.052
103
BNF002 Bone Fracture 47 0.052
104
c HMG001 Hemoglobin C Disease 47 0.052
105
SCR002 Scurvy 45 0.052
106
PRS036 Parasitic Protozoa Infectious Disease 45 0.052
107
c HMG003 Hemoglobin E Disease 44 0.052
108
ANC001 Ancylostomiasis 43 0.052
109
DYS015 Dysentery 41 0.052
110
BRB001 Beriberi 40 0.052
111
c PNC106 Pancreatic Agenesis 1 40 0.052
112
RCT017 Rectal Disease 39 0.052
113
ADJ001 Adjustment Disorder 38 0.052
114
CHR028 Chronic Wasting Disease 34 0.052
115
BTN004 Biotin Deficiency 33 0.052
116
c HMG004 Hemoglobin D Disease 33 0.052
117
ADS015 Aids Wasting Syndrome 18 0.052
118
P LNG032 Lung Cancer 94 0.043
119
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.043
120
P SCH015 Schizophrenia 76 0.043
121
CRH001 Crohn's Disease 76 0.043
122
P HRT032 Heart Disease 76 0.043
123
c DLT002 Dilated Cardiomyopathy 75 0.043
124
P NRV007 Nervous System Disease 71 0.043
125
P RSP003 Respiratory Failure 70 0.043
126
c HPT016 Hepatitis B 64 0.043
127
RSP006 Respiratory System Disease 62 0.043
128
TTN003 Tetanus 61 0.043
129
P LYM026 Lymphoblastic Leukemia 60 0.043
130
P NRP001 Neuropathy 60 0.043
131
VRL011 Viral Infectious Disease 59 0.043
132
MSS002 Mass Syndrome 59 0.043
133
ART021 Arteriosclerosis 59 0.043
134
CHL071 Child Syndrome 58 0.043
135
LPD008 Lipid Metabolism Disorder 58 0.043
136
SCH014 Schistosomiasis 58 0.043
137
P CTR002 Cataract 57 0.043
138
WLL006 Wells Syndrome 56 0.043
139
WLM001 Wolman Disease 56 0.043
140
DSS008 Disease of Mental Health 55 0.043
141
GST050 Gastrointestinal System Disease 54 0.043
142
GTR002 Goiter 54 0.043
143
GST037 Gastroparesis 53 0.043
144
ALL026 Allergic Hypersensitivity Disease 53 0.043
145
KDS001 Kid Syndrome 53 0.043
146
END035 Endocrine Gland Cancer 52 0.043
147
NTH001 Netherton Syndrome 52 0.043
148
P MSC003 Muscular Atrophy 51 0.043
149
c INF067 Inflammatory Bowel Disease 10 51 0.043
150
MCR094 Microvillus Inclusion Disease 51 0.043
151
PRC012 Pericardial Effusion 50 0.043
152
PRT030 Parathyroid Gland Disease 49 0.043
153
ALC009 Alcoholic Liver Cirrhosis 48 0.043
154
CRD002 Cri-Du-Chat Syndrome 48 0.043
155
SXL003 Sexual Disorder 47 0.043
156
RLP003 Relapsing Fever 46 0.043
157
TBR011 Tuberculous Meningitis 46 0.043
158
DNT012 Dental Caries 46 0.043
159
ALN001 Aland Island Eye Disease 45 0.043
160
AYM001 Ayme-Gripp Syndrome 45 0.043
161
GDS001 Good Syndrome 45 0.043
162
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.043
163
ANM001 Anemia of Prematurity 43 0.043
164
EXC002 Exocrine Pancreatic Insufficiency 43 0.043
165
END038 Endocrine Pancreas Disease 43 0.043
166
TRC023 Trichinosis 43 0.043
167
GST009 Gastroschisis 43 0.043
168
DNT001 Dental Fluorosis 43 0.043
169
P CRB088 Cerebral Atrophy 42 0.043
170
c CLR085 Colorectal Cancer 1 42 0.043
171
AMB001 Amebiasis 42 0.043
172
FTL021 Fetal Macrosomia 41 0.043
173
PSD029 Pseudocholinesterase Deficiency 40 0.043
174
SPR007 Superior Mesenteric Artery Syndrome 39 0.043
175
c HYP058 Hypervitaminosis a 38 0.043
176
RMN001 Rumination Disorder 38 0.043
177
PLC008 Placenta Disease 36 0.043
178
ALR002 Al-Raqad Syndrome 36 0.043
179
c CNG413 Congenital Short Bowel Syndrome 36 0.043
180
NCR001 Necrotizing Ulcerative Gingivitis 35 0.043
181
FNC006 Functional Gastric Disease 34 0.043
182
NNT011 Neonatal Anemia 34 0.043
183
c PNC111 Pancreatic Cancer 2 30 0.043
184
HNS001 Hansen's Disease 29 0.043
185
c PNC094 Pancreatic Cancer 1 29 0.043
186
c CRN214 Coronary Heart Disease 5 23 0.043
187
c DLT001 Delta Chain Disease 16 0.043
188
c SYS001 Systemic Lupus Erythematosus 87 0.030
189
HV1006 Hiv-1 82 0.030
190
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.030
191
DCH001 Duchenne Muscular Dystrophy 80 0.030
192
STR067 Stroke, Ischemic 77 0.030
193
GST053 Gastric Cancer 77 0.030
194
P HYP607 Hypercholesterolemia, Familial 77 0.030
195
P CRN211 Coronary Artery Disease 75 0.030
196
c HPT073 Hepatitis C Virus 72 0.030
197
P HMC003 Hemochromatosis 72 0.030
198
P LYM118 Lymphoma 70 0.030
199
c HYP595 Hypertension, Essential 69 0.030
200
PRP027 Peripheral Vascular Disease 69 0.030
201
SCK003 Sickle Cell Anemia 68 0.030
202
ISC006 Ischemic Heart Disease 68 0.030
203
SKN016 Skin Disease 68 0.030
204
PLM001 Pulmonary Tuberculosis 68 0.030
205
BCK001 Becker Muscular Dystrophy 68 0.030
206
P KDN017 Kidney Cancer 67 0.030
207
PCK002 Pick Disease 67 0.030
208
VSC007 Vascular Disease 67 0.030
209
c PNC108 Pancreatitis, Hereditary 67 0.030
210
OBS002 Obsessive-Compulsive Disorder 66 0.030
211
P MSC005 Muscular Dystrophy 64 0.030
212
WLM007 Wilms Tumor Susceptibility-5 64 0.030
213
P PRM019 Premature Ovarian Failure 64 0.030
214
P TRN020 Turner Syndrome 64 0.030
215
DMN002 Dementia 64 0.030
216
P AMY004 Amyloidosis 64 0.030
217
CHD001 Chediak-Higashi Syndrome 64 0.030
218
MTH009 Mouth Disease 63 0.030
219
P CRD013 Cardiofaciocutaneous Syndrome 63 0.030
220
P LPS004 Lupus Erythematosus 63 0.030
221
P PRT010 Parathyroid Carcinoma 62 0.030
222
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.030
223
BLM001 Bloom Syndrome 62 0.030
224
CHG001 Chagas Disease 62 0.030
225
GST092 Gastroesophageal Reflux 61 0.030
226
PRM097 Primary Immunodeficiency Disease 61 0.030
227
P ENC004 Encephalitis 61 0.030
228
P THL005 Thalassemia 61 0.030
229
HYP056 Hypoglycemia 61 0.030
230
ISB001 Isobutyryl-Coa Dehydrogenase Deficiency 60 0.030
231
GNG013 Gingivitis 60 0.030
232
HYP066 Hyperglycemia 60 0.030
233
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.030
234
OVR029 Ovarian Hyperstimulation Syndrome 60 0.030
235
GST045 Gastroenteritis 60 0.030
236
P ALC004 Alcohol Abuse 60 0.030
237
RBR001 Roberts Syndrome 59 0.030
238
P HRS035 Hirschsprung Disease 1 59 0.030
239
P ENC018 Encephalopathy 59 0.030
240
c HPT003 Hepatitis a 59 0.030
241
STT001 Status Epilepticus 59 0.030
242
P MCR010 Microcephaly 58 0.030
243
P ORL007 Oral Cavity Cancer 58 0.030
244
P PRC031 Preeclampsia/eclampsia 1 57 0.030
245
P HYP069 Hyperparathyroidism 57 0.030
246
P EXN002 Exanthem 57 0.030
247
P CND004 Candidiasis 57 0.030
248
c MSC124 Muscular Dystrophy, Congenital 57 0.030
249
ART111 Artery Disease 57 0.030
250
PPT005 Peptic Ulcer Disease 56 0.030
251
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.030
252
CND002 Conduct Disorder 56 0.030
253
CLF027 Cleft Palate, Isolated 56 0.030
254
P HYP076 Hyperthyroidism 56 0.030
255
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.030
256
ORL011 Oral Cancer 55 0.030
257
c HYP615 Hyperparathyroidism, Familial Primary 55 0.030
258
CHL014 Cholera 55 0.030
259
HYP266 Hypoxia 55 0.030
260
PRL032 Perlman Syndrome 55 0.030
261
GST023 Gastric Ulcer 55 0.030
262
GLC003 Glucose Intolerance 55 0.030
263
P LRY019 Laryngitis 55 0.030
264
c ANG041 Angioedema, Hereditary, Types I and Ii 55 0.030
265
c BCT007 Bacterial Meningitis 54 0.030
266
MNT002 Mental Depression 54 0.030
267
P ECL001 Eclampsia 54 0.030
268
PLS007 Plasmodium Falciparum Malaria 54 0.030
269
c VRL007 Viral Encephalitis 54 0.030
270
ACH005 Achalasia 54 0.030
271
P FRC002 Fructose Intolerance 53 0.030
272
c CNT075 Central Precocious Puberty 53 0.030
273
ADL002 Adult Syndrome 53 0.030
274
C3D001 C3 Deficiency 53 0.030
275
SHG001 Shigellosis 53 0.030
276
ESP023 Esophageal Disease 53 0.030
277
PLS006 Plasmodium Vivax Malaria 53 0.030
278
P FTL001 Fetal Alcohol Syndrome 53 0.030
279
P ANG015 Angioedema 53 0.030
280
P GND004 Gonadal Dysgenesis 53 0.030
281
P DGR001 Digeorge Syndrome 52 0.030
282
P LPD010 Lipodystrophy 52 0.030
283
c HPT015 Hepatitis D 52 0.030
284
P HYP083 Hypopituitarism 52 0.030
285
DBT062 Diabetic Foot Ulcers 52 0.030
286
P PNC001 Pancytopenia 52 0.030
287
HYP077 Hypertrichosis 52 0.030
288
BLR007 Biliary Tract Neoplasm 52 0.030
289
VND001 Vein Disease 52 0.030
290
CYS005 Cysticercosis 52 0.030
291
URC002 Urea Cycle Disorder 51 0.030
292
PRT011 Protein C Deficiency 51 0.030
293
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.030
294
P DDN001 Duodenal Ulcer 51 0.030
295
VND002 Van Der Woude Syndrome 51 0.030
296
P PRC019 Precocious Puberty 51 0.030
297
OCL008 Oculopharyngeal Muscular Dystrophy 51 0.030
298
ADT003 Auditory System Disease 51 0.030
299
HPT074 Hepatic Adenoma, Somatic 51 0.030
300
P FML035 Familial Hyperlipidemia 50 0.030
301
MRC001 Marchiafava Bignami Disease 50 0.030
302
IMM136 Immune System Disease 50 0.030
303
DYS014 Dyspepsia 50 0.030
304
ONC002 Onchocerciasis 50 0.030
305
PLC005 Placental Insufficiency 50 0.030
306
MGC001 Megacolon 50 0.030
307
LYS003 Lysinuric Protein Intolerance 50 0.030
308
RTN023 Retinitis 49 0.030
309
P CHR345 Chronic Pain 49 0.030
310
GRW007 Growth Hormone Deficiency 48 0.030
311
P SHR001 Short Bowel Syndrome 48 0.030
312
OBS001 Obstructive Jaundice 48 0.030
313
GLT021 Glutaricaciduria, Type I 48 0.030
314
TRC008 Trachoma 48 0.030
315
WHP001 Whipple Disease 48 0.030
316
CRB025 Carbohydrate Metabolic Disorder 47 0.030
317
BCT004 Bacteriuria 47 0.030
318
CRD118 Cardiovascular Cancer 47 0.030
319
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.030
320
INT067 Interstitial Nephritis 47 0.030
321
LKC003 Leukocyte Disease 47 0.030
322
c INT072 Intestinal Pseudo-Obstruction 46 0.030
323
RPR002 Reproductive System Disease 46 0.030
324
ACR041 Acromelic Frontonasal Dysostosis 46 0.030
325
P PRD008 Periodontitis 46 0.030
326
P TRC086 Trichohepatoenteric Syndrome 1 46 0.030
327
ACT058 Active Peptic Ulcer Disease 46 0.030
328
DWR001 Dwarfism 46 0.030
329
P TCL004 T-Cell Leukemia 46 0.030
330
CRB004 Cerebral Artery Occlusion 46 0.030
331
SKN023 Skin Tag 46 0.030
332
SCB001 Scabies 45 0.030
333
BNC003 Bone Cancer 45 0.030
334
RNL097 Renal Artery Disease 45 0.030
335
HMS001 Hemosiderosis 45 0.030
336
TCL003 T Cell Deficiency 45 0.030
337
BWN001 Bowen-Conradi Syndrome 45 0.030
338
SKN027 Skin Conditions 45 0.030
339
CRR007 Cirrhosis, Cryptogenic 44 0.030
340
PHY002 Physical Disorder 44 0.030
341
MLK006 Milk Allergy 44 0.030
342
P SDR002 Siderosis 44 0.030
343
GLS007 Glossitis 44 0.030
344
HYP085 Hypothalamic Disease 44 0.030
345
WRN003 Wernicke Encephalopathy 44 0.030
346
ATX003 Ataxia with Isolated Vitamin E Deficiency 44 0.030
347
BRT030 Birth Defects 43 0.030
348
IRN002 Iron Metabolism Disease 43 0.030
349
DRR008 Diarrhea 1, Secretory Chloride, Congenital 43 0.030
350
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.030
351
AMN006 Aminoaciduria 42 0.030
352
THL018 Thalassemia Major 42 0.030
353
END072 Endotheliitis 42 0.030
354
IMP004 Impetigo 42 0.030
355
ESN004 Eosinophilic Gastritis 42 0.030
356
CNT025 Central Pontine Myelinolysis 42 0.030
357
TNS007 Taeniasis 42 0.030
358
MCR017 Macrocytic Anemia 41 0.030
359
P HVY001 Heavy Chain Disease 41 0.030
360
HYP081 Hypolipoproteinemia 41 0.030
361
SCN001 Secondary Hyperparathyroidism of Renal Origin 41 0.030
362
P FML187 Familial Hypertension 41 0.030
363
c PRG106 Progressive Muscular Dystrophy 41 0.030
364
NM001 Noma 41 0.030
365
c CHR096 Chronic Pulmonary Heart Disease 40 0.030
366
ESP025 Esophagus Adenocarcinoma 40 0.030
367
STT004 Steatorrhea 40 0.030
368
ESP018 Esophageal Candidiasis 40 0.030
369
SPC003 Specific Developmental Disorder 40 0.030
370
c PRM212 Primary Microcephaly 39 0.030
371
ASP004 Asphyxia Neonatorum 39 0.030
372
NSY001 N Syndrome 39 0.030
373
PYM001 Pyomyositis 39 0.030
374
C1N001 C1 Inhibitor Deficiency 39 0.030
375
PRT035 Peritoneum Cancer 39 0.030
376
TRC077 Trichomegaly 38 0.030
377
ALC010 Alcoholic Cardiomyopathy 38 0.030
378
MCR020 Microsporidiosis 38 0.030
379
HTS001 Hiatus Hernia 38 0.030
380
ASP008 Aspiration Pneumonitis 38 0.030
381
GNR003 Generalized Atherosclerosis 38 0.030
382
SNL007 Senile Cataract 38 0.030
383
P RTN022 Retinal Vein Occlusion 37 0.030
384
JJN008 Jejunoileitis 37 0.030
385
c ACQ005 Acquired Thrombocytopenia 37 0.030
386
LRY017 Laryngeal Disease 37 0.030
387
SPL040 Split Hand 37 0.030
388
PPT002 Peptic Ulcer Perforation 37 0.030
389
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 36 0.030
390
SML020 Small Patella Syndrome 36 0.030
391
PYR016 Pyridoxine Deficiency 36 0.030
392
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 36 0.030
393
VTM001 Vitamin K Deficiency Hemorrhagic Disease 36 0.030
394
ANR018 Anorchia 36 0.030
395
CRV026 Cervical Clear Cell Adenocarcinoma 36 0.030
396
PRP080 Peripheral Artery Disease 36 0.030
397
c CNT016 Central Retinal Vein Occlusion 35 0.030
398
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.030
399
PPT001 Peptic Esophagitis 35 0.030
400
CCN007 Cocoon Syndrome 35 0.030
401
PNC028 Pancreatic Steatorrhea 35 0.030
402
ECT004 Ecthyma 35 0.030
403
MYP100 Myopathy, X-Linked, with Excessive Autophagy 35 0.030
404
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 35 0.030
405
ACD004 Acdc 34 0.030
406
FLC001 Folic Acid Deficiency Anemia 34 0.030
407
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.030
408
PYR004 Pyuria 34 0.030
409
ACR005 Acrodermatitis 34 0.030
410
c CRD187 Cardiomyopathy, Dilated, 3b 34 0.030
411
DDN007 Duodenal Disease 34 0.030
412
c HYP311 Hyperparathyroidism 3 34 0.030
413
ISC001 Ischemic Neuropathy 33 0.030
414
VTM003 Vitamin Metabolic Disorder 33 0.030
415
RFR013 Refractory Celiac Disease 33 0.030
416
ANS012 Anus Disease 32 0.030
417
BRL001 Brill-Zinsser Disease 32 0.030
418
IMM068 Immunodeficiency 8 32 0.030
419
MTC061 Mitochondrial Dna Depletion Syndrome 1 32 0.030
420
GST004 Gastric Neuroendocrine Neoplasm 32 0.030
421
SKL007 Skeletal Muscle Regeneration 32 0.030
422
WHT017 Wheat Allergy 32 0.030
423
c INF002 Inflammatory Diarrhea 31 0.030
424
CRB031 Cerebral Arterial Disease 31 0.030
425
PNM003 Pneumatosis Cystoides Intestinalis 31 0.030
426
LWR004 Lower Urinary Tract Calculus 31 0.030
427
c CHR057 Chronic Laryngitis 31 0.030
428
SQM005 Squamous Papillomatosis 31 0.030
429
ATR073 Atrophic Glossitis 31 0.030
430
BLD041 Bladder Calculus 31 0.030
431
NNT005 Neonatal Candidiasis 30 0.030
432
c ACT072 Acute Laryngitis 30 0.030
433
FSH003 Fish Allergy 30 0.030
434
TMP011 Temple-Baraitser Syndrome 30 0.030
435
PHT004 Photoallergic Dermatitis 30 0.030
436
LRY007 Laryngeal Tuberculosis 29 0.030
437
c ANR038 Anorexia Nervosa 1 29 0.030
438
CHR067 Chronic Intestinal Vascular Insufficiency 29 0.030
439
IDP034 Idiopathic Central Precocious Puberty 29 0.030
440
OSM001 Osmotic Diarrhea 29 0.030
441
FNG003 Fungal Esophagitis 28 0.030
442
ANS018 Anismus 28 0.030
443
MCL069 Macular Dystrophy, Retinal, 1, North Carolina Type 27 0.030
444
OST097 Osteoporotic Fracture 27 0.030
445
GRN011 Granulomatous Gastritis 27 0.030
446
SCR037 Sucrase-Isomaltase Deficiency, Congenital 27 0.030
447
MRG013 Mirage Syndrome 26 0.030
448
c PRC047 Precocious Puberty, Central, 1 26 0.030
449
P KLZ004 Kala-Azar 1 26 0.030
450
GST090 Gastroduodenal Crohn's Disease 25 0.030
451
FCL001 Facial Dermatosis 25 0.030
452
c GST091 Gastrointestinal Neuroendocrine Benign Tumor 24 0.030
453
CMB002 Combat Disorder 24 0.030
454
CRB087 Cerebral Arteriosclerosis 24 0.030
455
MTC055 Mitochondrial Dna Depletion Syndrome 4b 24 0.030
456
SPS090 Sepsis in Premature Infants 23 0.030
457
MXD019 Mixed Malaria 23 0.030
458
c INF093 Inflammatory Bowel Disease 14 23 0.030
459
c ALP087 Alpha-Heavy Chain Disease 23 0.030
460
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 23 0.030
461
c CLC048 Celiac Disease 3 22 0.030
462
P INT103 Intrauterine Infections 22 0.030
463
MSC012 Muscular Dystrophy, Duchenne and Becker Type 22 0.030
464
c CLC037 Celiac Disease 4 22 0.030
465
CNG101 Congenital Human Immunodeficiency Virus 21 0.030
466
MND006 Mondor Disease 21 0.030
467
c HYP290 Hypobetalipoproteinemia, Familial, 2 21 0.030
468
EXC004 Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis 21 0.030
469
PYR009 Pyridoxine Deficiency Anemia 21 0.030
470
GLT030 Gluten Allergy 20 0.030
471
c INF079 Inflammatory Bowel Disease 20 20 0.030
472
c CLC039 Celiac Disease 13 20 0.030
473
c PRC033 Preeclampsia/eclampsia 3 19 0.030
474
VSC049 Visceral Myopathy, Familial, with External Ophthalmoplegia 19 0.030
475
ATR076 Atrophic Muscular Disease 18 0.030
476
GST088 Gastric Endocrine Tumor 17 0.030
477
HYP481 Hyperbiliverdinemia 17 0.030
478
NDD001 Nodding Syndrome 17 0.030
479
c KLZ002 Kala-Azar 2 16 0.030
480
CMP052 Complication in Hemodialysis 16 0.030
481
CHY005 Chylothorax, Congenital 15 0.030
482
WST006 Westphal Disease 11 0.030
483
HYP680 Hypoglossia with Situs Inversus Hypoglossia, Isolated, Included 11 0.030
484
SPL043 Split Hand, Bilateral 10 0.030