Search results for "malnutrition"

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

284 hits were found for 'malnutrition'

# Family MCID Name MIFTS Score
1
PRT038 Protein-Energy Malnutrition 48 7.592
2
PRC002 Paracoccidioidomycosis 68 2.702
3
KWS001 Kwashiorkor 48 0.226
4
PRT036 Peritonitis 72 0.172
5
c HPT021 Hepatitis 64 0.155
6
MRS001 Marasmus 47 0.146
7
c PNC044 Pancreatitis 69 0.130
8
XRP001 Xerophthalmia 38 0.125
9
P OBS005 Obesity 91 0.119
10
c DRR001 Diarrhea 52 0.119
11
P MLR004 Malaria 75 0.113
12
P ANR007 Anorexia Nervosa 66 0.113
13
c THY032 Thyroiditis 66 0.113
14
LVR012 Liver Cirrhosis 77 0.106
15
c DBT009 Diabetes Mellitus 74 0.106
16
ATH003 Atherosclerosis 69 0.106
17
ASC002 Ascariasis 47 0.106
18
CYS001 Cystic Fibrosis 97 0.099
19
ALC006 Alcoholic Hepatitis 58 0.099
20
URM002 Uremia 58 0.099
21
GRD001 Giardiasis 57 0.099
22
P PLL002 Pellagra 55 0.099
23
P LKM002 Leukemia 77 0.092
24
ISC004 Ischemia 63 0.092
25
TRP004 Tropical Sprue 38 0.092
26
P ART022 Arthritis 75 0.084
27
MSL001 Measles 68 0.084
28
P INS005 Insulin Resistance 65 0.084
29
PRT019 Protein-Losing Enteropathy 51 0.084
30
MTB004 Metabolic Acidosis 45 0.084
31
CRB009 Cerebritis 39 0.084
32
P RHM011 Rheumatoid Arthritis 94 0.075
33
TBR010 Tuberculosis 87 0.075
34
P RCK004 Rickets 68 0.075
35
c KDN018 Kidney Disease 63 0.075
36
c ACT073 Acute Leukemia 57 0.075
37
DYS073 Dysphagia 52 0.075
38
P LCT002 Lactose Intolerance 49 0.075
39
ANC001 Ancylostomiasis 40 0.075
40
CRH001 Crohn's Disease 76 0.065
41
ACQ007 Acquired Immunodeficiency Syndrome 71 0.065
42
P NRB001 Neuroblastoma 70 0.065
43
P LVR013 Liver Disease 69 0.065
44
c MNN013 Meningitis 68 0.065
45
MRB003 Morbid Obesity 68 0.065
46
P ESP024 Esophagitis 64 0.065
47
CRB021 Cerebral Malaria 60 0.065
48
ETN001 Eating Disorder 57 0.065
49
FDL002 Food Allergy 53 0.065
50
HYP037 Hyperhomocysteinemia 53 0.065
51
BRN080 Brain Ischemia 51 0.065
52
DYS015 Dysentery 51 0.065
53
OVR063 Overnutrition 49 0.065
54
c NGH001 Night Blindness 49 0.065
55
DBT061 Diabetic Nephropathy 47 0.065
56
BRB001 Beriberi 45 0.065
57
c ACT004 Acute Diarrhea 44 0.065
58
BTN004 Biotin Deficiency 42 0.065
59
P DLT002 Dilated Cardiomyopathy 88 0.053
60
P HYP075 Hypertension 87 0.053
61
P SCH015 Schizophrenia 82 0.053
62
P LNG032 Lung Cancer 79 0.053
63
CNG034 Congestive Heart Failure 78 0.053
64
P PNM007 Pneumonia 78 0.053
65
LSH001 Leishmaniasis 74 0.053
66
SCH014 Schistosomiasis 72 0.053
67
P INF038 Influenza 68 0.053
68
GST009 Gastroschisis 66 0.053
69
c JVN010 Juvenile Rheumatoid Arthritis 66 0.053
70
P CHR089 Chronic Kidney Failure 66 0.053
71
P WLM002 Wilms Tumor 66 0.053
72
TTN003 Tetanus 65 0.053
73
c VRL010 Viral Hepatitis 64 0.053
74
DFC004 Deficiency Anemia 63 0.053
75
P ACT101 Acute Lymphoblastic Leukemia 63 0.053
76
P GTR002 Goiter 62 0.053
77
NRP001 Neuropathy 62 0.053
78
VSC003 Visceral Leishmaniasis 61 0.053
79
AMB001 Amebiasis 60 0.053
80
TBR011 Tuberculous Meningitis 59 0.053
81
PRC012 Pericardial Effusion 58 0.053
82
END030 End Stage Renal Failure 58 0.053
83
PRT039 Proteinuria 58 0.053
84
P SDR002 Siderosis 58 0.053
85
BRN071 Brain Injury 58 0.053
86
IRN001 Iron Deficiency Anemia 57 0.053
87
c CTR002 Cataract 57 0.053
88
c LYM026 Lymphoblastic Leukemia 57 0.053
89
c HYP060 Hyperinsulinism 57 0.053
90
P CHR409 Chronic Obstructive Pulmonary Disease 54 0.053
91
P INT072 Intestinal Pseudo-Obstruction 54 0.053
92
BLN003 Blindness 53 0.053
93
ALC009 Alcoholic Liver Cirrhosis 52 0.053
94
OBS001 Obstructive Jaundice 51 0.053
95
BRN106 Burns 50 0.053
96
DNT001 Dental Fluorosis 49 0.053
97
DNT012 Dental Caries 49 0.053
98
P HYP058 Hypervitaminosis a 49 0.053
99
KRT002 Keratomalacia 48 0.053
100
FTL021 Fetal Macrosomia 45 0.053
101
CRB088 Cerebral Atrophy 44 0.053
102
HLM001 Helminthiasis 43 0.053
103
c INF037 Inflammatory Bowel Disease 40 0.053
104
TRC023 Trichinosis 40 0.053
105
NTR005 Nutritional Deficiency Disease 33 0.053
106
NCR001 Necrotizing Ulcerative Gingivitis 30 0.053
107
P ALZ001 Alzheimer's Disease 100 0.038
108
P LVR011 Liver Cancer 91 0.038
109
P SYS001 Systemic Lupus Erythematosus 88 0.038
110
P ATX002 Ataxia Telangiectasia 87 0.038
111
GLC006 Galactosemia 86 0.038
112
P HMC003 Hemochromatosis 83 0.038
113
SCK003 Sickle Cell Anemia 82 0.038
114
AND002 Androgen Insensitivity Syndrome 80 0.038
115
c NNN003 Noonan Syndrome 80 0.038
116
P PRC016 Pre-Eclampsia 78 0.038
117
BRK003 Burkitt's Lymphoma 77 0.038
118
P CLR023 Colorectal Cancer 77 0.038
119
ANK002 Ankylosing Spondylitis 77 0.038
120
c LPS004 Lupus Erythematosus 77 0.038
121
LRN002 Laron Syndrome 77 0.038
122
CHD001 Chediak-Higashi Syndrome 76 0.038
123
P OST002 Osteoporosis 76 0.038
124
BLM001 Bloom Syndrome 74 0.038
125
c PRM002 Primary Hyperoxaluria 74 0.038
126
P WGN002 Wegener's Granulomatosis 74 0.038
127
P CLC005 Celiac Disease 73 0.038
128
OBS002 Obsessive-Compulsive Disorder 73 0.038
129
HYP458 Hyper Ige Syndrome 72 0.038
130
c THL005 Thalassemia 72 0.038
131
DBT011 Diabetic Retinopathy 71 0.038
132
P ANG001 Angelman Syndrome 70 0.038
133
P MTB001 Metabolic Syndrome X 70 0.038
134
VSC007 Vascular Disease 70 0.038
135
c ACT074 Acute Lymphocytic Leukemia 70 0.038
136
TRC008 Trachoma 70 0.038
137
SPS077 Sepsis 70 0.038
138
ADN001 Adenosine Deaminase Deficiency 70 0.038
139
c HPT016 Hepatitis B 70 0.038
140
P CNG401 Congenital Heart Disease 69 0.038
141
P PLY011 Polycystic Ovary Syndrome 68 0.038
142
ART021 Arteriosclerosis 68 0.038
143
P AMY004 Amyloidosis 68 0.038
144
c NPH012 Nephrotic Syndrome 67 0.038
145
c AXN002 Axenfeld-Rieger Syndrome 67 0.038
146
P HYP056 Hypoglycemia 67 0.038
147
P DGR001 Digeorge Syndrome 67 0.038
148
P HRD011 Hereditary Spherocytosis 67 0.038
149
P HPT001 Hepatitis C 67 0.038
150
P PRD008 Periodontitis 67 0.038
151
OVR029 Ovarian Hyperstimulation Syndrome 67 0.038
152
STT001 Status Epilepticus 66 0.038
153
P MCL015 Mucolipidosis Ii 66 0.038
154
P OVR049 Ovarian Disease 66 0.038
155
SHG001 Shigellosis 65 0.038
156
c ECL001 Eclampsia 64 0.038
157
ART019 Aortic Valve Stenosis 64 0.038
158
CRY003 Cryptosporidiosis 64 0.038
159
CHL014 Cholera 64 0.038
160
OCL008 Oculopharyngeal Muscular Dystrophy 64 0.038
161
c GLL020 Gallbladder Disease 64 0.038
162
HV1006 Hiv-1 64 0.038
163
STF001 Stiff-Person Syndrome 64 0.038
164
c HYP076 Hyperthyroidism 64 0.038
165
CMP002 Campylobacteriosis 63 0.038
166
CHG001 Chagas Disease 63 0.038
167
ACN002 Acanthosis Nigricans 63 0.038
168
CYS005 Cysticercosis 63 0.038
169
BTN003 Biotinidase Deficiency 63 0.038
170
HYP066 Hyperglycemia 62 0.038
171
TRN001 Transthyretin Amyloidosis 62 0.038
172
P CRD013 Cardiofaciocutaneous Syndrome 62 0.038
173
RBS003 Rabson-Mendenhall Syndrome 62 0.038
174
TYP007 Typhoid Fever 62 0.038
175
MYL020 Myelomeningocele 62 0.038
176
P CND004 Candidiasis 62 0.038
177
c FML012 Familial Partial Lipodystrophy 62 0.038
178
GLC003 Glucose Intolerance 62 0.038
179
GNG013 Gingivitis 61 0.038
180
PLM001 Pulmonary Tuberculosis 61 0.038
181
SCB001 Scabies 61 0.038
182
MGC001 Megacolon 60 0.038
183
BLM002 Bulimia Nervosa 59 0.038
184
LPD010 Lipodystrophy 59 0.038
185
BCT004 Bacteriuria 59 0.038
186
SCR002 Scurvy 58 0.038
187
P INT068 Intestinal Disease 58 0.038
188
c CNT016 Central Retinal Vein Occlusion 58 0.038
189
HYP266 Hypoxia 58 0.038
190
HMS001 Hemosiderosis 57 0.038
191
P RTN022 Retinal Vein Occlusion 57 0.038
192
INS008 Insulin-Like Growth Factor I Deficiency 56 0.038
193
CRD005 Cardia Cancer 56 0.038
194
ACR005 Acrodermatitis 55 0.038
195
PRM003 Premature Ejaculation 55 0.038
196
ART001 Arterial Tortuosity Syndrome 55 0.038
197
VND002 Van Der Woude Syndrome 55 0.038
198
HPT023 Hepatocellular Carcinoma 54 0.038
199
c ACR001 Aicardi-Goutieres Syndrome 54 0.038
200
SCH012 Schizoaffective Disorder 54 0.038
201
STT004 Steatorrhea 54 0.038
202
RTN023 Retinitis 54 0.038
203
AND003 Andersen-Tawil Syndrome 54 0.038
204
P MSC003 Muscular Atrophy 54 0.038
205
GST045 Gastroenteritis 54 0.038
206
MCR010 Microcephaly 53 0.038
207
P HYP083 Hypopituitarism 53 0.038
208
YLL001 Yellow Nail Syndrome 53 0.038
209
c CNG012 Congenital Generalized Lipodystrophy 53 0.038
210
NM001 Noma 53 0.038
211
P PRP023 Peripheral Neuropathy 52 0.038
212
THR013 Thoracic Outlet Syndrome 52 0.038
213
ESN005 Eosinophilic Gastroenteritis 52 0.038
214
ONC002 Onchocerciasis 52 0.038
215
URC002 Urea Cycle Disorder 52 0.038
216
HVD003 Hiv/aids 52 0.038
217
GLS007 Glossitis 52 0.038
218
AMY053 Amyloidosis, Secondary 52 0.038
219
SHR001 Short Bowel Syndrome 52 0.038
220
P ALC004 Alcohol Abuse 52 0.038
221
LPD004 Lipoid Nephrosis 51 0.038
222
P CST002 Castleman's Disease 51 0.038
223
END072 Endotheliitis 51 0.038
224
c TCL004 T-Cell Leukemia 51 0.038
225
SMT019 Somatostatin Analog 51 0.038
226
MCR020 Microsporidiosis 50 0.038
227
P NRV007 Nervous System Disease 50 0.038
228
c BCT007 Bacterial Meningitis 50 0.038
229
ATX019 Ataxia with Vitamin E Deficiency 50 0.038
230
HYP077 Hypertrichosis 50 0.038
231
c SVR005 Severe Pre-Eclampsia 49 0.038
232
IMP004 Impetigo 49 0.038
233
ALC010 Alcoholic Cardiomyopathy 49 0.038
234
EXC002 Exocrine Pancreatic Insufficiency 49 0.038
235
MCR094 Microvillus Inclusion Disease 48 0.038
236
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 48 0.038
237
TRN022 Transcobalamin Ii Deficiency 47 0.038
238
CNT025 Central Pontine Myelinolysis 47 0.038
239
BNF002 Bone Fracture 45 0.038
240
MCR017 Macrocytic Anemia 45 0.038
241
c FTL001 Fetal Alcohol Syndrome 45 0.038
242
LPT005 Leptin Deficiency 45 0.038
243
FBR063 Fibrocalculous Pancreatic Diabetes 45 0.038
244
FTT001 Fatty Liver Disease 44 0.038
245
PLC005 Placental Insufficiency 44 0.038
246
AMN006 Aminoaciduria 44 0.038
247
HYP029 Hyperthyroxinemia 43 0.038
248
SNL007 Senile Cataract 43 0.038
249
P ATX010 Ataxia Neuropathy Spectrum 43 0.038
250
5FL001 5-Fluorouracil Toxicity 42 0.038
251
WRN003 Wernicke Encephalopathy 41 0.038
252
ESP028 Esophageal Squamous Cell Carcinoma 41 0.038
253
c HVY001 Heavy Chain Disease 39 0.038
254
c MLR021 Malaria, Severe 39 0.038
255
VRL011 Viral Infectious Disease 39 0.038
256
SPR066 Superficial Siderosis 38 0.038
257
PLT008 Pili Torti 38 0.038
258
SML020 Small Patella Syndrome 37 0.038
259
c HYP290 Hypobetalipoproteinemia, Familial, 2 37 0.038
260
IPX001 Ipex Syndrome 37 0.038
261
VSC044 Visceral Myopathy 37 0.038
262
NRT005 North Carolina Macular Dystrophy 37 0.038
263
DYS070 Dysalbuminemic Hyperthyroxinemia 36 0.038
264
PYR016 Pyridoxine Deficiency 36 0.038
265
SYN053 Syndromic Diarrhea 34 0.038
266
PSD029 Pseudocholinesterase Deficiency 34 0.038
267
CNG127 Congenital Sucrase-Isomaltase Deficiency 32 0.038
268
P ATS059 Autosomal Dominant Hyper Ige Syndrome 31 0.038
269
c ALP060 Alpha Heavy-Chain Disease 30 0.038
270
ANK010 Ankylostomiasis 29 0.038
271
PYR004 Pyuria 28 0.038
272
TFT003 Tufting Enteropathy 28 0.038
273
TNS007 Taeniasis 28 0.038
274
HNM002 Hinman Syndrome 28 0.038
275
ECT004 Ecthyma 28 0.038
276
IRN002 Iron Metabolism Disease 28 0.038
277
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.038
278
BNT002 Bantu Siderosis 26 0.038
279
ATR073 Atrophic Glossitis 24 0.038
280
MNT002 Mental Depression 23 0.038
281
c BNG076 Benign Exophthalmos Syndrome 22 0.038
282
HYP081 Hypolipoproteinemia 19 0.038
283
BRL001 Brill-Zinsser Disease 19 0.038
284
HYP481 Hyperbiliverdinemia 15 0.038