Search results for "malnutrition"

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

486 hits were found for 'malnutrition'

# Family MCID Name MIFTS Score
1
PRT038 Protein-Energy Malnutrition 48 7.274
2
NTR005 Nutritional Deficiency Disease 51 3.252
3
KWS001 Kwashiorkor 45 0.202
4
P DRR001 Diarrhea 60 0.175
5
MRS001 Marasmus 39 0.147
6
PRT036 Peritonitis 65 0.141
7
MLR004 Malaria 80 0.134
8
P HPT021 Hepatitis 74 0.134
9
c ACT004 Acute Diarrhea 38 0.131
10
P PNC044 Pancreatitis 62 0.120
11
P OBS005 Obesity 91 0.104
12
ACD009 Acid-Labile Subunit, Deficiency of 37 0.104
13
ATH003 Atherosclerosis 63 0.100
14
XRP001 Xerophthalmia 36 0.100
15
c DRR009 Diarrhea 6 30 0.100
16
DFC004 Deficiency Anemia 64 0.095
17
INS024 Insulin-Like Growth Factor I 75 0.095
18
P ANR007 Anorexia Nervosa 63 0.095
19
P THY032 Thyroiditis 57 0.095
20
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.090
21
LVR012 Liver Cirrhosis 71 0.090
22
MSL001 Measles 61 0.090
23
ETN001 Eating Disorder 59 0.090
24
P PNM007 Pneumonia 67 0.090
25
CYS001 Cystic Fibrosis 87 0.085
26
P KDN018 Kidney Disease 64 0.085
27
ASC002 Ascariasis 38 0.085
28
GRD001 Giardiasis 40 0.085
29
ALC006 Alcoholic Hepatitis 60 0.085
30
ISC004 Ischemia 56 0.085
31
P LVR013 Liver Disease 76 0.079
32
TBR010 Tuberculosis 70 0.079
33
P LKM002 Leukemia 70 0.079
34
P INF038 Influenza 71 0.079
35
LPD004 Lipoid Nephrosis 49 0.079
36
URM002 Uremia 36 0.079
37
P ART022 Arthritis 73 0.074
38
c CHR089 Chronic Kidney Failure 67 0.074
39
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.074
40
IRN001 Iron Deficiency Anemia 51 0.074
41
P NGH001 Night Blindness 49 0.074
42
TRP004 Tropical Sprue 36 0.074
43
P PLL002 Pellagra 43 0.074
44
FDL002 Food Allergy 56 0.074
45
PRT019 Protein-Losing Enteropathy 42 0.074
46
CRB009 Cerebritis 36 0.074
47
P RHM011 Rheumatoid Arthritis 87 0.067
48
P CLR023 Colorectal Cancer 96 0.067
49
P RCK004 Rickets 59 0.067
50
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.067
51
c HPT001 Hepatitis C 68 0.067
52
DYS073 Dysphagia 51 0.067
53
SPC010 Speech and Communication Disorders 42 0.067
54
LCT002 Lactose Intolerance 45 0.067
55
ADM013 Adamantinoma of Long Bones 57 0.067
56
c ACT073 Acute Leukemia 61 0.067
57
END030 End Stage Renal Failure 53 0.067
58
MTB004 Metabolic Acidosis 49 0.067
59
FNC002 Functional Diarrhea 39 0.067
60
BRN080 Brain Ischemia 42 0.067
61
MSC004 Muscle Tissue Disease 35 0.067
62
P NRB001 Neuroblastoma 70 0.060
63
CNG034 Congestive Heart Failure 72 0.060
64
KRT002 Keratomalacia 50 0.060
65
CHY002 Chylomicron Retention Disease 54 0.060
66
LSH001 Leishmaniasis 63 0.060
67
P MNN013 Meningitis 66 0.060
68
P ESP024 Esophagitis 62 0.060
69
P GST049 Gastrointestinal System Cancer 59 0.060
70
P CRD011 Cardiomyopathy 66 0.060
71
STM006 Stomach Disease 48 0.060
72
VSC003 Visceral Leishmaniasis 56 0.060
73
P INT068 Intestinal Disease 60 0.060
74
c VRL010 Viral Hepatitis 60 0.060
75
c DRR007 Diarrhea 7 32 0.060
76
MRB003 Morbid Obesity 59 0.060
77
CLN019 Colonic Disease 50 0.060
78
P HYP060 Hyperinsulinism 58 0.060
79
INT253 Intestinal Benign Neoplasm 48 0.060
80
BTN004 Biotin Deficiency 34 0.060
81
BLD054 Blood Protein Disease 38 0.060
82
IMP003 Impaired Renal Function Disease 36 0.060
83
BNS002 Bone Structure Disease 37 0.060
84
BRN071 Brain Injury 51 0.060
85
BRN106 Burns 52 0.060
86
P PNC035 Pancreatic Cancer 86 0.052
87
P OST002 Osteoporosis 63 0.052
88
P CLC005 Celiac Disease 67 0.052
89
CRD002 Cri-Du-Chat Syndrome 48 0.052
90
c DLT002 Dilated Cardiomyopathy 75 0.052
91
VSC044 Visceral Myopathy 44 0.052
92
CRH001 Crohn's Disease 76 0.052
93
RSP006 Respiratory System Disease 61 0.052
94
NTH001 Netherton Syndrome 52 0.052
95
P URF003 Urofacial Syndrome 1 51 0.052
96
PSD029 Pseudocholinesterase Deficiency 40 0.052
97
CSY001 C Syndrome 49 0.052
98
c JVN010 Juvenile Rheumatoid Arthritis 65 0.052
99
RCT018 Rectal Neoplasm 53 0.052
100
P MYP004 Myopathy 67 0.052
101
TTN003 Tetanus 62 0.052
102
GTR002 Goiter 54 0.052
103
ANC001 Ancylostomiasis 43 0.052
104
PNC034 Pancreas Disease 56 0.052
105
P LYM026 Lymphoblastic Leukemia 60 0.052
106
ACQ007 Acquired Immunodeficiency Syndrome 60 0.052
107
CRY003 Cryptosporidiosis 47 0.052
108
BRB001 Beriberi 40 0.052
109
DNT012 Dental Caries 45 0.052
110
P SPS003 Spastic Diplegia 49 0.052
111
LRN003 Learning Disability 49 0.052
112
c HMG003 Hemoglobin E Disease 44 0.052
113
ALR002 Al-Raqad Syndrome 36 0.052
114
c PNC106 Pancreatic Agenesis 1 31 0.052
115
c INF067 Inflammatory Bowel Disease 10 31 0.052
116
RCT017 Rectal Disease 35 0.052
117
PRC012 Pericardial Effusion 50 0.052
118
DYS015 Dysentery 42 0.052
119
ADJ001 Adjustment Disorder 38 0.052
120
ALC009 Alcoholic Liver Cirrhosis 53 0.052
121
HYP037 Hyperhomocysteinemia 49 0.052
122
P CRB088 Cerebral Atrophy 40 0.052
123
TBR011 Tuberculous Meningitis 46 0.052
124
PRS036 Parasitic Protozoa Infectious Disease 45 0.052
125
CHR028 Chronic Wasting Disease 33 0.052
126
c HYP058 Hypervitaminosis a 35 0.052
127
BNM008 Bone Mineral Density, Low 28 0.052
128
OVR063 Overnutrition 49 0.052
129
FNC006 Functional Gastric Disease 33 0.052
130
ADS015 Aids Wasting Syndrome 14 0.052
131
FTL021 Fetal Macrosomia 38 0.052
132
BNF002 Bone Fracture 46 0.052
133
P LNG032 Lung Cancer 92 0.042
134
HPT023 Hepatocellular Carcinoma 90 0.042
135
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.042
136
P SCH015 Schizophrenia 78 0.042
137
SKN016 Skin Disease 69 0.042
138
WLM007 Wilms Tumor Susceptibility-5 64 0.042
139
P RSP003 Respiratory Failure 68 0.042
140
WLM001 Wolman Disease 55 0.042
141
c PNC108 Pancreatitis, Hereditary 59 0.042
142
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.042
143
GST092 Gastroesophageal Reflux 62 0.042
144
CLF027 Cleft Palate, Isolated 56 0.042
145
VND002 Van Der Woude Syndrome 50 0.042
146
P NRV007 Nervous System Disease 71 0.042
147
VRL011 Viral Infectious Disease 56 0.042
148
MCR094 Microvillus Inclusion Disease 49 0.042
149
PRL032 Perlman Syndrome 55 0.042
150
c CNG401 Congenital Heart Disease 67 0.042
151
CHL071 Child Syndrome 58 0.042
152
GST023 Gastric Ulcer 56 0.042
153
AMB001 Amebiasis 43 0.042
154
PPT005 Peptic Ulcer Disease 58 0.042
155
PRP027 Peripheral Vascular Disease 69 0.042
156
c HPT016 Hepatitis B 61 0.042
157
P MCR010 Microcephaly 60 0.042
158
SCR002 Scurvy 47 0.042
159
MSS002 Mass Syndrome 49 0.042
160
TMP011 Temple-Baraitser Syndrome 34 0.042
161
ESP023 Esophageal Disease 52 0.042
162
MYP100 Myopathy, X-Linked, with Excessive Autophagy 37 0.042
163
KDS001 Kid Syndrome 53 0.042
164
SML020 Small Patella Syndrome 36 0.042
165
SCH014 Schistosomiasis 59 0.042
166
LPD008 Lipid Metabolism Disorder 42 0.042
167
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 39 0.042
168
HPT074 Hepatic Adenoma, Somatic 35 0.042
169
GST037 Gastroparesis 54 0.042
170
MCL069 Macular Dystrophy, Retinal, 1, North Carolina Type 27 0.042
171
c CNG413 Congenital Short Bowel Syndrome 34 0.042
172
ASP008 Aspiration Pneumonitis 39 0.042
173
DRR008 Diarrhea 1, Secretory Chloride, Congenital 42 0.042
174
P DDN001 Duodenal Ulcer 51 0.042
175
EXT034 Extrinsic Allergic Alveolitis 58 0.042
176
NCR001 Necrotizing Ulcerative Gingivitis 37 0.042
177
ALN001 Aland Island Eye Disease 45 0.042
178
TRC023 Trichinosis 44 0.042
179
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.042
180
ACT058 Active Peptic Ulcer Disease 44 0.042
181
WLL006 Wells Syndrome 57 0.042
182
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.042
183
CND002 Conduct Disorder 54 0.042
184
PRT030 Parathyroid Gland Disease 49 0.042
185
PLC008 Placenta Disease 33 0.042
186
RMN001 Rumination Disorder 33 0.042
187
c PNC111 Pancreatic Cancer 2 33 0.042
188
GST002 Gastric Mucosal Hypertrophy 35 0.042
189
AYM001 Ayme-Gripp Syndrome 40 0.042
190
c PNC094 Pancreatic Cancer 1 27 0.042
191
P KLZ004 Kala-Azar 1 25 0.042
192
c HMG001 Hemoglobin C Disease 46 0.042
193
P CTR002 Cataract 57 0.042
194
c ANR038 Anorexia Nervosa 1 28 0.042
195
ART021 Arteriosclerosis 59 0.042
196
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.042
197
c CLR085 Colorectal Cancer 1 39 0.042
198
SKN027 Skin Conditions 44 0.042
199
END035 Endocrine Gland Cancer 50 0.042
200
DNT001 Dental Fluorosis 42 0.042
201
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 19 0.042
202
P MSC033 Muscle Disorders 52 0.042
203
PPT001 Peptic Esophagitis 35 0.042
204
SPR007 Superior Mesenteric Artery Syndrome 37 0.042
205
INT067 Interstitial Nephritis 48 0.042
206
HTS001 Hiatus Hernia 40 0.042
207
RLP003 Relapsing Fever 40 0.042
208
DSS008 Disease of Mental Health 48 0.042
209
c CRN214 Coronary Heart Disease 5 22 0.042
210
GDS001 Good Syndrome 46 0.042
211
SXL003 Sexual Disorder 45 0.042
212
P LRY019 Laryngitis 55 0.042
213
GST090 Gastroduodenal Crohn's Disease 26 0.042
214
P NRP001 Neuropathy 57 0.042
215
DYS014 Dyspepsia 50 0.042
216
LWR004 Lower Urinary Tract Calculus 30 0.042
217
ESP018 Esophageal Candidiasis 40 0.042
218
EXC002 Exocrine Pancreatic Insufficiency 41 0.042
219
NNT005 Neonatal Candidiasis 30 0.042
220
GST009 Gastroschisis 31 0.042
221
LRY017 Laryngeal Disease 33 0.042
222
JJN008 Jejunoileitis 38 0.042
223
PNC028 Pancreatic Steatorrhea 34 0.042
224
ESP025 Esophagus Adenocarcinoma 42 0.042
225
c ACT072 Acute Laryngitis 37 0.042
226
ANM001 Anemia of Prematurity 44 0.042
227
c CHR057 Chronic Laryngitis 30 0.042
228
CHR067 Chronic Intestinal Vascular Insufficiency 28 0.042
229
LRY007 Laryngeal Tuberculosis 29 0.042
230
PPT002 Peptic Ulcer Perforation 36 0.042
231
BLD041 Bladder Calculus 29 0.042
232
ESN004 Eosinophilic Gastritis 41 0.042
233
PHT004 Photoallergic Dermatitis 29 0.042
234
NNT011 Neonatal Anemia 34 0.042
235
HNS001 Hansen's Disease 30 0.042
236
c HMG004 Hemoglobin D Disease 32 0.042
237
CHN003 Chondroblastic Osteosarcoma 38 0.042
238
PNM003 Pneumatosis Cystoides Intestinalis 32 0.042
239
END038 Endocrine Pancreas Disease 42 0.042
240
CRV026 Cervical Clear Cell Adenocarcinoma 34 0.042
241
ISC001 Ischemic Neuropathy 33 0.042
242
GRN011 Granulomatous Gastritis 28 0.042
243
FNG003 Fungal Esophagitis 27 0.042
244
SQM005 Squamous Papillomatosis 29 0.042
245
c DLT001 Delta Chain Disease 14 0.042
246
ANS018 Anismus 25 0.042
247
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.030
248
c HYP595 Hypertension, Essential 69 0.030
249
STR067 Stroke, Ischemic 74 0.030
250
P STM004 Stomach Cancer 73 0.030
251
P HYP607 Hypercholesterolemia, Familial 77 0.030
252
c SYS001 Systemic Lupus Erythematosus 87 0.030
253
SCK003 Sickle Cell Anemia 72 0.030
254
HV1006 Hiv-1 80 0.030
255
P HMC003 Hemochromatosis 71 0.030
256
P CRN211 Coronary Artery Disease 74 0.030
257
OBS002 Obsessive-Compulsive Disorder 66 0.030
258
P KDN017 Kidney Cancer 67 0.030
259
P PRM019 Premature Ovarian Failure 65 0.030
260
GLT021 Glutaricaciduria, Type I 47 0.030
261
ANM029 Anemia, Sideroblastic, X-Linked 53 0.030
262
DCH001 Duchenne Muscular Dystrophy 81 0.030
263
WLL001 Williams-Beuren Syndrome 61 0.030
264
LYS003 Lysinuric Protein Intolerance 51 0.030
265
CHD001 Chediak-Higashi Syndrome 66 0.030
266
RBR001 Roberts Syndrome 61 0.030
267
BLM001 Bloom Syndrome 63 0.030
268
BCK001 Becker Muscular Dystrophy 68 0.030
269
P CRD013 Cardiofaciocutaneous Syndrome 65 0.030
270
c MSC124 Muscular Dystrophy, Congenital 57 0.030
271
STT001 Status Epilepticus 59 0.030
272
GST050 Gastrointestinal System Disease 58 0.030
273
P TRN020 Turner Syndrome 64 0.030
274
ADT003 Auditory System Disease 49 0.030
275
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.030
276
P ZLL001 Zellweger Syndrome 49 0.030
277
P TRC086 Trichohepatoenteric Syndrome 1 46 0.030
278
P PRC031 Preeclampsia/eclampsia 1 53 0.030
279
OCL008 Oculopharyngeal Muscular Dystrophy 50 0.030
280
P PRT010 Parathyroid Carcinoma 61 0.030
281
P PRC019 Precocious Puberty 53 0.030
282
SCR037 Sucrase-Isomaltase Deficiency, Congenital 26 0.030
283
P DGR001 Digeorge Syndrome 52 0.030
284
MTC061 Mitochondrial Dna Depletion Syndrome 1 31 0.030
285
IRR002 Irritable Bowel Syndrome 58 0.030
286
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.030
287
CRB039 Cerebrovascular Disease 49 0.030
288
SHG001 Shigellosis 52 0.030
289
ADL002 Adult Syndrome 53 0.030
290
P FRC002 Fructose Intolerance 54 0.030
291
ACH005 Achalasia 55 0.030
292
c MTB001 Metabolic Syndrome X 61 0.030
293
P LPS004 Lupus Erythematosus 63 0.030
294
MTH009 Mouth Disease 63 0.030
295
OVR029 Ovarian Hyperstimulation Syndrome 59 0.030
296
MTC055 Mitochondrial Dna Depletion Syndrome 4b 23 0.030
297
ALL026 Allergic Hypersensitivity Disease 53 0.030
298
HYP077 Hypertrichosis 52 0.030
299
P LYM118 Lymphoma 68 0.030
300
HYP066 Hyperglycemia 61 0.030
301
P MSC005 Muscular Dystrophy 64 0.030
302
c HRD002 Hereditary Angioedema 52 0.030
303
c CRD187 Cardiomyopathy, Dilated, 3b 40 0.030
304
c HPT073 Hepatitis C Virus 72 0.030
305
P THL005 Thalassemia 61 0.030
306
c INT072 Intestinal Pseudo-Obstruction 45 0.030
307
TRC008 Trachoma 50 0.030
308
c HPT015 Hepatitis D 51 0.030
309
GNG013 Gingivitis 61 0.030
310
IMM102 Immunodeficiency 14 33 0.030
311
BNC003 Bone Cancer 44 0.030
312
URC002 Urea Cycle Disorder 52 0.030
313
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 36 0.030
314
HYP056 Hypoglycemia 60 0.030
315
CYS005 Cysticercosis 52 0.030
316
BWN001 Bowen-Conradi Syndrome 51 0.030
317
VSC007 Vascular Disease 51 0.030
318
TRC077 Trichomegaly 40 0.030
319
BLR007 Biliary Tract Neoplasm 49 0.030
320
PLS007 Plasmodium Falciparum Malaria 56 0.030
321
P HYP076 Hyperthyroidism 59 0.030
322
CHG001 Chagas Disease 62 0.030
323
P ECL001 Eclampsia 55 0.030
324
P ORL007 Oral Cavity Cancer 58 0.030
325
c PRM005 Primary Hyperparathyroidism 56 0.030
326
c HPT003 Hepatitis a 55 0.030
327
EXC004 Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis 22 0.030
328
IMM068 Immunodeficiency 8 32 0.030
329
SCB001 Scabies 45 0.030
330
ONC002 Onchocerciasis 53 0.030
331
P ENC018 Encephalopathy 59 0.030
332
VSC049 Visceral Myopathy, Familial, with External Ophthalmoplegia 20 0.030
333
WHP001 Whipple Disease 49 0.030
334
c PRC016 Pre-Eclampsia 57 0.030
335
CHL014 Cholera 56 0.030
336
PLS006 Plasmodium Vivax Malaria 52 0.030
337
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 40 0.030
338
ANS012 Anus Disease 32 0.030
339
RPR002 Reproductive System Disease 45 0.030
340
LNG099 Lung Disease 63 0.030
341
ATX003 Ataxia with Isolated Vitamin E Deficiency 36 0.030
342
P HYP069 Hyperparathyroidism 57 0.030
343
P CND004 Candidiasis 58 0.030
344
P ENC004 Encephalitis 60 0.030
345
c HYP290 Hypobetalipoproteinemia, Familial, 2 20 0.030
346
c HYP311 Hyperparathyroidism 3 33 0.030
347
P HRT032 Heart Disease 64 0.030
348
P ANG015 Angioedema 53 0.030
349
GST045 Gastroenteritis 59 0.030
350
LMB010 Lambert Syndrome 35 0.030
351
CNT025 Central Pontine Myelinolysis 43 0.030
352
NSY001 N Syndrome 42 0.030
353
SKN023 Skin Tag 48 0.030
354
P HYP083 Hypopituitarism 50 0.030
355
PLM001 Pulmonary Tuberculosis 69 0.030
356
DWR001 Dwarfism 42 0.030
357
P GND004 Gonadal Dysgenesis 51 0.030
358
ASP004 Asphyxia Neonatorum 38 0.030
359
FCL001 Facial Dermatosis 24 0.030
360
CRB025 Carbohydrate Metabolic Disorder 46 0.030
361
P PRD008 Periodontitis 46 0.030
362
NM001 Noma 42 0.030
363
HYP481 Hyperbiliverdinemia 17 0.030
364
IMP004 Impetigo 41 0.030
365
MRC001 Marchiafava Bignami Disease 33 0.030
366
P MSC003 Muscular Atrophy 51 0.030
367
P FML035 Familial Hyperlipidemia 49 0.030
368
CCN007 Cocoon Syndrome 32 0.030
369
MGC001 Megacolon 50 0.030
370
WRN003 Wernicke Encephalopathy 42 0.030
371
IRN002 Iron Metabolism Disease 38 0.030
372
PYM001 Pyomyositis 39 0.030
373
VND001 Vein Disease 51 0.030
374
FML039 Female Reproductive System Disease 49 0.030
375
P SHR001 Short Bowel Syndrome 51 0.030
376
c CLC037 Celiac Disease 4 20 0.030
377
c CLC048 Celiac Disease 3 21 0.030
378
c PRC047 Precocious Puberty, Central, 1 25 0.030
379
MCR020 Microsporidiosis 38 0.030
380
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.030
381
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.030
382
TNS007 Taeniasis 41 0.030
383
GLS007 Glossitis 46 0.030
384
c BCT007 Bacterial Meningitis 55 0.030
385
P AMY004 Amyloidosis 63 0.030
386
GLC003 Glucose Intolerance 56 0.030
387
MNT002 Mental Depression 52 0.030
388
BCT004 Bacteriuria 48 0.030
389
c CNT075 Central Precocious Puberty 49 0.030
390
HYP081 Hypolipoproteinemia 42 0.030
391
MCR017 Macrocytic Anemia 43 0.030
392
C1N001 C1 Inhibitor Deficiency 38 0.030
393
P PNC001 Pancytopenia 53 0.030
394
ANR018 Anorchia 35 0.030
395
HMS001 Hemosiderosis 42 0.030
396
c INF093 Inflammatory Bowel Disease 14 22 0.030
397
HYP085 Hypothalamic Disease 43 0.030
398
P ALC004 Alcohol Abuse 57 0.030
399
BRL001 Brill-Zinsser Disease 26 0.030
400
PYR004 Pyuria 33 0.030
401
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.030
402
AMN006 Aminoaciduria 39 0.030
403
OBS001 Obstructive Jaundice 47 0.030
404
ATR073 Atrophic Glossitis 30 0.030
405
P SDR002 Siderosis 44 0.030
406
c CLC039 Celiac Disease 13 19 0.030
407
HMN014 Human Immunodeficiency Virus Infectious Disease 46 0.030
408
P PLT008 Pili Torti 19 0.030
409
P FTL001 Fetal Alcohol Syndrome 53 0.030
410
GRW007 Growth Hormone Deficiency 49 0.030
411
ACD004 Acdc 35 0.030
412
FLC001 Folic Acid Deficiency Anemia 34 0.030
413
ALC010 Alcoholic Cardiomyopathy 38 0.030
414
VTM001 Vitamin K Deficiency Hemorrhagic Disease 37 0.030
415
PRT035 Peritoneum Cancer 34 0.030
416
OGL001 Ogilvie Syndrome 17 0.030
417
MLK006 Milk Allergy 50 0.030
418
STT004 Steatorrhea 41 0.030
419
P LPD010 Lipodystrophy 51 0.030
420
ISC006 Ischemic Heart Disease 54 0.030
421
LKC003 Leukocyte Disease 45 0.030
422
GST053 Gastric Cancer 52 0.030
423
P HVY001 Heavy Chain Disease 41 0.030
424
DBT062 Diabetic Foot Ulcers 55 0.030
425
DDN007 Duodenal Disease 34 0.030
426
PYR016 Pyridoxine Deficiency 28 0.030
427
HYP680 Hypoglossia with Situs Inversus Hypoglossia, Isolated, Included 11 0.030
428
ORL011 Oral Cancer 53 0.030
429
ART111 Artery Disease 56 0.030
430
HYP266 Hypoxia 55 0.030
431
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.030
432
GNR003 Generalized Atherosclerosis 35 0.030
433
c ALP087 Alpha-Heavy Chain Disease 23 0.030
434
SPC003 Specific Developmental Disorder 39 0.030
435
SPL040 Split Hand 35 0.030
436
WHT017 Wheat Allergy 38 0.030
437
PLC005 Placental Insufficiency 50 0.030
438
PYR009 Pyridoxine Deficiency Anemia 20 0.030
439
CMB002 Combat Disorder 22 0.030
440
CNG101 Congenital Human Immunodeficiency Virus 21 0.030
441
ACR005 Acrodermatitis 33 0.030
442
CLC007 Calcium Metabolism Disease 39 0.030
443
c CNT016 Central Retinal Vein Occlusion 34 0.030
444
ECT004 Ecthyma 37 0.030
445
RNL097 Renal Artery Disease 44 0.030
446
MXD019 Mixed Malaria 22 0.030
447
P TCL004 T-Cell Leukemia 44 0.030
448
WST006 Westphal Disease 11 0.030
449
c PRM212 Primary Microcephaly 38 0.030
450
c CRN174 Coronary Heart Disease 2 19 0.030
451
GLC008 Glucose Metabolism Disease 44 0.030
452
c KLZ002 Kala-Azar 2 14 0.030
453
c PRC033 Preeclampsia/eclampsia 3 17 0.030
454
PRP080 Peripheral Artery Disease 35 0.030
455
NDD001 Nodding Syndrome 16 0.030
456
SNL007 Senile Cataract 37 0.030
457
P CHR345 Chronic Pain 45 0.030
458
TCL003 T Cell Deficiency 44 0.030
459
c PRG106 Progressive Muscular Dystrophy 40 0.030
460
MSC012 Muscular Dystrophy, Duchenne and Becker Type 21 0.030
461
RTN023 Retinitis 49 0.030
462
SPS090 Sepsis in Premature Infants 22 0.030
463
c INF079 Inflammatory Bowel Disease 20 19 0.030
464
RFR013 Refractory Celiac Disease 32 0.030
465
OSM001 Osmotic Diarrhea 28 0.030
466
P RTN022 Retinal Vein Occlusion 36 0.030
467
CRB031 Cerebral Arterial Disease 31 0.030
468
FSH003 Fish Allergy 29 0.030
469
GLT030 Gluten Allergy 19 0.030
470
CRB004 Cerebral Artery Occlusion 39 0.030
471
c INF002 Inflammatory Diarrhea 31 0.030
472
MND006 Mondor Disease 20 0.030
473
c CHR096 Chronic Pulmonary Heart Disease 40 0.030
474
IDP034 Idiopathic Central Precocious Puberty 27 0.030
475
CRB087 Cerebral Arteriosclerosis 23 0.030
476
CMP052 Complication in Hemodialysis 14 0.030
477
END072 Endotheliitis 41 0.030
478
MRG013 Mirage Syndrome 11 0.030
479
SKL007 Skeletal Muscle Regeneration 31 0.030
480
SPL043 Split Hand, Bilateral 8 0.030
481
THL018 Thalassemia Major 31 0.030
482
VTM003 Vitamin Metabolic Disorder 31 0.030
483
P FML187 Familial Hypertension 35 0.030
484
GST088 Gastric Endocrine Tumor 16 0.030
485
P INT103 Intrauterine Infections 21 0.030
486
OST097 Osteoporotic Fracture 25 0.030