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

355 hits were found for 'malnutrition'

# Family MCID Name MIFTS Score
1
PRT038 Protein-Energy Malnutrition 53 7.417
2
PRC002 Paracoccidioidomycosis 70 2.741
3
KWS001 Kwashiorkor 47 0.209
4
LPT005 Leptin Deficiency 30 0.168
5
PRT036 Peritonitis 78 0.161
6
MRS001 Marasmus 44 0.146
7
c HPT021 Hepatitis 75 0.141
8
BNZ002 Benzene Toxicity 26 0.128
9
P ANR007 Anorexia Nervosa 67 0.124
10
c PNC044 Pancreatitis 67 0.119
11
SDR002 Siderosis 53 0.119
12
VTM002 Vitamin B12 Deficiency 51 0.119
13
TBR011 Tuberculous Meningitis 40 0.119
14
ACD008 Acid-Labile Subunit Deficiency 30 0.119
15
c DRR001 Diarrhea 54 0.114
16
XRP001 Xerophthalmia 35 0.114
17
SPR066 Superficial Siderosis 26 0.114
18
IRN001 Iron Deficiency Anemia 61 0.108
19
P PLL002 Pellagra 52 0.108
20
PCH007 Pouchitis 40 0.108
21
BRG002 Berger Disease 27 0.108
22
P STR035 Streptococcal Group a Invasive Disease 14 0.108
23
P OBS005 Obesity 93 0.103
24
LRN002 Laron Syndrome 76 0.103
25
P MLR004 Malaria 73 0.103
26
c THY032 Thyroiditis 67 0.103
27
MYL020 Myelomeningocele 47 0.103
28
GRW007 Growth Hormone Deficiency 39 0.103
29
RDT013 Radiation Proctitis 33 0.103
30
FTL021 Fetal Macrosomia 32 0.103
31
PYR016 Pyridoxine Deficiency 21 0.103
32
c DBT009 Diabetes Mellitus 80 0.097
33
LVR012 Liver Cirrhosis 75 0.097
34
ATH003 Atherosclerosis 71 0.097
35
CRB009 Cerebritis 56 0.097
36
P INS005 Insulin Resistance 48 0.097
37
ASC002 Ascariasis 47 0.097
38
VND002 Van Der Woude Syndrome 43 0.097
39
CYS001 Cystic Fibrosis 103 0.091
40
P LKM002 Leukemia 79 0.091
41
ALC006 Alcoholic Hepatitis 57 0.091
42
EGG001 Egg Allergy 54 0.091
43
GRD001 Giardiasis 54 0.091
44
HYP459 Hyperferritinemia Cataract Syndrome 44 0.091
45
ISC004 Ischemia 64 0.084
46
URM002 Uremia 56 0.084
47
P NGH001 Night Blindness 53 0.084
48
P HRM005 Hermansky-Pudlak Syndrome 1 51 0.084
49
ESN005 Eosinophilic Gastroenteritis 47 0.084
50
NNL002 Nonalcoholic Steatohepatitis 39 0.084
51
c CNT075 Central Precocious Puberty 36 0.084
52
TRP004 Tropical Sprue 35 0.084
53
CNG034 Congestive Heart Failure 81 0.077
54
P ART022 Arthritis 75 0.077
55
ANK002 Ankylosing Spondylitis 75 0.077
56
MSL001 Measles 66 0.077
57
ACQ007 Acquired Immunodeficiency Syndrome 63 0.077
58
P OVR049 Ovarian Disease 63 0.077
59
c ACT073 Acute Leukemia 62 0.077
60
P HRD057 Hereditary Pancreatitis 53 0.077
61
P LCT002 Lactose Intolerance 50 0.077
62
MTB004 Metabolic Acidosis 49 0.077
63
PRT019 Protein-Losing Enteropathy 48 0.077
64
ANC001 Ancylostomiasis 43 0.077
65
PRL042 Proliferating Trichilemmal Cyst 38 0.077
66
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 36 0.077
67
DYS070 Dysalbuminemic Hyperthyroxinemia 26 0.077
68
TFT003 Tufting Enteropathy 21 0.077
69
P ATX002 Ataxia Telangiectasia 93 0.069
70
P RHM011 Rheumatoid Arthritis 91 0.069
71
TBR010 Tuberculosis 84 0.069
72
CRH001 Crohn's Disease 83 0.069
73
PRC016 Pre-Eclampsia 75 0.069
74
P INF038 Influenza 69 0.069
75
c LCL006 Localized Scleroderma 68 0.069
76
P RCK004 Rickets 67 0.069
77
EXT034 Extrinsic Allergic Alveolitis 65 0.069
78
STF001 Stiff-Person Syndrome 60 0.069
79
CRB021 Cerebral Malaria 59 0.069
80
c KDN018 Kidney Disease 58 0.069
81
PLY013 Polymyalgia Rheumatica 56 0.069
82
SCN006 Secondary Syphilis 55 0.069
83
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 53 0.069
84
CNG048 Congenital Hepatic Fibrosis 53 0.069
85
BTN004 Biotin Deficiency 41 0.069
86
c ACT004 Acute Diarrhea 35 0.069
87
c ICH041 Ichthyosis, Autosomal Recessive 4b 31 0.069
88
NRT005 North Carolina Macular Dystrophy 28 0.069
89
HNM002 Hinman Syndrome 24 0.069
90
HV1007 Hiv1 Infection 23 0.069
91
HRL001 Harlequin Type Ichthyosis 22 0.069
92
HPT023 Hepatocellular Carcinoma 89 0.059
93
P DLT002 Dilated Cardiomyopathy 82 0.059
94
LSH001 Leishmaniasis 74 0.059
95
c MNN013 Meningitis 71 0.059
96
P NRB001 Neuroblastoma 71 0.059
97
P LVR013 Liver Disease 70 0.059
98
MRB003 Morbid Obesity 68 0.059
99
P PLY011 Polycystic Ovary Syndrome 68 0.059
100
P HRD011 Hereditary Spherocytosis 66 0.059
101
c NPH012 Nephrotic Syndrome 66 0.059
102
ETN001 Eating Disorder 63 0.059
103
c VRL010 Viral Hepatitis 61 0.059
104
P GTR002 Goiter 61 0.059
105
FDL002 Food Allergy 60 0.059
106
c HPT003 Hepatitis a 60 0.059
107
P ESP024 Esophagitis 60 0.059
108
INT075 Intracranial Hypertension 59 0.059
109
P ALC004 Alcohol Abuse 57 0.059
110
HYP037 Hyperhomocysteinemia 55 0.059
111
DBT061 Diabetic Nephropathy 54 0.059
112
THR013 Thoracic Outlet Syndrome 54 0.059
113
P MSC003 Muscular Atrophy 52 0.059
114
c MLR021 Malaria, Severe 49 0.059
115
KRT002 Keratomalacia 47 0.059
116
c CNG013 Congenital Disorder of Glycosylation Type I 46 0.059
117
CHL079 Children's Interstitial Lung Disease 46 0.059
118
DYS015 Dysentery 45 0.059
119
OVR063 Overnutrition 44 0.059
120
BRB001 Beriberi 43 0.059
121
CHL039 Choledocholithiasis 43 0.059
122
ENT001 Enterocele 42 0.059
123
CNG116 Congenital Nephrotic Syndrome Finnish Type 39 0.059
124
RTC003 Root Caries 36 0.059
125
ERL004 Early Yaws 33 0.059
126
c TTL001 Total Internal Ophthalmoplegia 17 0.059
127
P HYP075 Hypertension 86 0.049
128
P PNM007 Pneumonia 79 0.049
129
P SCH015 Schizophrenia 77 0.049
130
P TRN020 Turner Syndrome 77 0.049
131
BRN024 Bronchitis 76 0.049
132
P CHR089 Chronic Kidney Failure 76 0.049
133
P LNG032 Lung Cancer 74 0.049
134
ACN002 Acanthosis Nigricans 73 0.049
135
SCH014 Schistosomiasis 72 0.049
136
RLP001 Relapsing Polychondritis 69 0.049
137
IRR002 Irritable Bowel Syndrome 68 0.049
138
c JVN010 Juvenile Rheumatoid Arthritis 67 0.049
139
DFC004 Deficiency Anemia 66 0.049
140
P HMP002 Hemophagocytic Lymphohistiocytosis 66 0.049
141
HYP458 Hyper Ige Syndrome 65 0.049
142
BRN106 Burns 64 0.049
143
TTN003 Tetanus 63 0.049
144
c ACT027 Acute Pancreatitis 63 0.049
145
GLC003 Glucose Intolerance 63 0.049
146
P INT068 Intestinal Disease 61 0.049
147
VSC003 Visceral Leishmaniasis 61 0.049
148
NRP001 Neuropathy 61 0.049
149
HPT019 Hepatic Encephalopathy 58 0.049
150
P HYP083 Hypopituitarism 58 0.049
151
c ACT071 Acute Kidney Failure 58 0.049
152
PRT039 Proteinuria 57 0.049
153
P LYM026 Lymphoblastic Leukemia 56 0.049
154
RBS003 Rabson-Mendenhall Syndrome 56 0.049
155
AMB001 Amebiasis 56 0.049
156
c HYP060 Hyperinsulinism 56 0.049
157
ATX019 Ataxia with Vitamin E Deficiency 55 0.049
158
BNF002 Bone Fracture 55 0.049
159
ALC009 Alcoholic Liver Cirrhosis 55 0.049
160
PRC012 Pericardial Effusion 54 0.049
161
c CTR002 Cataract 53 0.049
162
DNT012 Dental Caries 51 0.049
163
P ALV004 Alveolar Rhabdomyosarcoma 51 0.049
164
P INF037 Inflammatory Bowel Disease 50 0.049
165
SCR002 Scurvy 49 0.049
166
c ACR001 Aicardi-Goutieres Syndrome 49 0.049
167
TRC023 Trichinosis 48 0.049
168
EXC002 Exocrine Pancreatic Insufficiency 47 0.049
169
ACT040 Acute Poststreptococcal Glomerulonephritis 46 0.049
170
TRN022 Transcobalamin Ii Deficiency 45 0.049
171
c CHR098 Chronic Pyelonephritis 44 0.049
172
DNT001 Dental Fluorosis 44 0.049
173
c VRL005 Viral Pneumonia 43 0.049
174
P INT072 Intestinal Pseudo-Obstruction 42 0.049
175
P HYP058 Hypervitaminosis a 42 0.049
176
DCB001 Decubitus Ulcer 39 0.049
177
IPX001 Ipex Syndrome 39 0.049
178
c ATM007 Autoimmune Disease of Central Nervous System 38 0.049
179
c RSM001 Rasmussen Encephalitis 37 0.049
180
CRB088 Cerebral Atrophy 33 0.049
181
SML020 Small Patella Syndrome 30 0.049
182
NCR001 Necrotizing Ulcerative Gingivitis 28 0.049
183
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.049
184
DYS073 Dysphagia 28 0.049
185
NTR005 Nutritional Deficiency Disease 28 0.049
186
NNS006 Non-Suppurative Otitis Media 26 0.049
187
P ALZ001 Alzheimer's Disease 103 0.034
188
GLC006 Galactosemia 93 0.034
189
AND002 Androgen Insensitivity Syndrome 88 0.034
190
P SYS001 Systemic Lupus Erythematosus 87 0.034
191
AGR001 Age Related Macular Degeneration 83 0.034
192
BLM001 Bloom Syndrome 82 0.034
193
P HMC003 Hemochromatosis 80 0.034
194
BRK003 Burkitt's Lymphoma 78 0.034
195
P ACT074 Acute Lymphocytic Leukemia 77 0.034
196
P OST002 Osteoporosis 77 0.034
197
c NNN003 Noonan Syndrome 77 0.034
198
ADN001 Adenosine Deaminase Deficiency 76 0.034
199
P WGN002 Wegener's Granulomatosis 75 0.034
200
P CRD013 Cardiofaciocutaneous Syndrome 74 0.034
201
OBS002 Obsessive-Compulsive Disorder 73 0.034
202
SCK003 Sickle Cell Anemia 73 0.034
203
c LPS004 Lupus Erythematosus 73 0.034
204
P CLC005 Celiac Disease 73 0.034
205
P CLR023 Colorectal Cancer 73 0.034
206
P CNG026 Congenital Heart Defect 73 0.034
207
VSC007 Vascular Disease 72 0.034
208
OVR029 Ovarian Hyperstimulation Syndrome 70 0.034
209
P ANG001 Angelman Syndrome 70 0.034
210
DBT001 Diabetic Ketoacidosis 69 0.034
211
c PRM002 Primary Hyperoxaluria 68 0.034
212
ART019 Aortic Valve Stenosis 68 0.034
213
c THL005 Thalassemia 68 0.034
214
P MTB001 Metabolic Syndrome X 67 0.034
215
VSC011 Vasculitis 67 0.034
216
P DGR001 Digeorge Syndrome 67 0.034
217
GNG013 Gingivitis 67 0.034
218
STT001 Status Epilepticus 66 0.034
219
P GLM007 Glomerulonephritis 66 0.034
220
P HPT001 Hepatitis C 66 0.034
221
P PRD008 Periodontitis 66 0.034
222
HYP056 Hypoglycemia 66 0.034
223
CHG001 Chagas Disease 66 0.034
224
P AMY004 Amyloidosis 65 0.034
225
ART021 Arteriosclerosis 65 0.034
226
HYP066 Hyperglycemia 65 0.034
227
c HPT016 Hepatitis B 65 0.034
228
P CMP010 Complex Regional Pain Syndrome 65 0.034
229
P PCH001 Pachyonychia Congenita 64 0.034
230
CYS005 Cysticercosis 64 0.034
231
WST001 West Syndrome 64 0.034
232
TRC008 Trachoma 64 0.034
233
P TRN001 Transthyretin Amyloidosis 64 0.034
234
BTN003 Biotinidase Deficiency 64 0.034
235
SHG001 Shigellosis 63 0.034
236
ECL001 Eclampsia 63 0.034
237
GST009 Gastroschisis 63 0.034
238
P CND004 Candidiasis 63 0.034
239
TYP007 Typhoid Fever 63 0.034
240
PLM001 Pulmonary Tuberculosis 63 0.034
241
BLM002 Bulimia Nervosa 62 0.034
242
c MCL015 Mucolipidosis Ii 62 0.034
243
ART001 Arterial Tortuosity Syndrome 62 0.034
244
CHL067 Cholecystitis 62 0.034
245
BRN029 Brain Disease 62 0.034
246
RTN023 Retinitis 61 0.034
247
FTT001 Fatty Liver Disease 61 0.034
248
c HYP076 Hyperthyroidism 61 0.034
249
OCL008 Oculopharyngeal Muscular Dystrophy 61 0.034
250
CHL014 Cholera 61 0.034
251
SQM006 Squamous Cell Carcinoma 61 0.034
252
CRY003 Cryptosporidiosis 60 0.034
253
c AXN002 Axenfeld-Rieger Syndrome 60 0.034
254
P RTN022 Retinal Vein Occlusion 59 0.034
255
INT051 Intussusception 59 0.034
256
LPD010 Lipodystrophy 59 0.034
257
c GLL020 Gallbladder Disease 59 0.034
258
CMP002 Campylobacteriosis 59 0.034
259
HNT002 Hantavirus Pulmonary Syndrome 57 0.034
260
c HRM001 Hermansky-Pudlak Syndrome 57 0.034
261
P SHR002 Short Stature 57 0.034
262
SCH012 Schizoaffective Disorder 57 0.034
263
MGC001 Megacolon 56 0.034
264
ONC002 Onchocerciasis 56 0.034
265
HYP068 Hyperostosis 56 0.034
266
SHR001 Short Bowel Syndrome 55 0.034
267
PNH001 Panhypopituitarism 55 0.034
268
BCT004 Bacteriuria 55 0.034
269
c BCT007 Bacterial Meningitis 54 0.034
270
c INT070 Intestinal Obstruction 54 0.034
271
HYP043 Hyperandrogenism 54 0.034
272
MCR010 Microcephaly 53 0.034
273
c CNT016 Central Retinal Vein Occlusion 53 0.034
274
PRP023 Peripheral Neuropathy 53 0.034
275
CRD005 Cardia Cancer 53 0.034
276
YLL001 Yellow Nail Syndrome 52 0.034
277
ADL002 Adult Syndrome 52 0.034
278
SVR005 Severe Pre-Eclampsia 52 0.034
279
TCL003 T Cell Deficiency 52 0.034
280
HMS001 Hemosiderosis 52 0.034
281
END030 End Stage Renal Failure 52 0.034
282
PRC003 Proctitis 51 0.034
283
HYP077 Hypertrichosis 51 0.034
284
ANV001 Anovulation 51 0.034
285
CHL004 Cholelithiasis 51 0.034
286
OBS001 Obstructive Jaundice 51 0.034
287
WRN002 Wernicke-Korsakoff Syndrome 51 0.034
288
SCB001 Scabies 51 0.034
289
ACR006 Aceruloplasminemia 51 0.034
290
STT004 Steatorrhea 50 0.034
291
IRN002 Iron Metabolism Disease 50 0.034
292
c TCL004 T-Cell Leukemia 49 0.034
293
MST005 Mastitis 49 0.034
294
ALC010 Alcoholic Cardiomyopathy 48 0.034
295
GLS007 Glossitis 47 0.034
296
MCR020 Microsporidiosis 47 0.034
297
SNL007 Senile Cataract 46 0.034
298
ACR005 Acrodermatitis 45 0.034
299
HPT008 Hepatic Tuberculosis 45 0.034
300
IMP004 Impetigo 45 0.034
301
PLC005 Placental Insufficiency 44 0.034
302
c CNG012 Congenital Generalized Lipodystrophy 44 0.034
303
WRN003 Wernicke Encephalopathy 44 0.034
304
P ATX010 Ataxia Neuropathy Spectrum 44 0.034
305
MCR017 Macrocytic Anemia 44 0.034
306
c FTL001 Fetal Alcohol Syndrome 44 0.034
307
c MLT074 Multiple Endocrine Neoplasia 43 0.034
308
MNN017 Mononeuropathy 43 0.034
309
AND003 Andersen-Tawil Syndrome 43 0.034
310
BRN071 Brain Injury 43 0.034
311
AMY053 Amyloidosis, Secondary 43 0.034
312
LPD004 Lipoid Nephrosis 42 0.034
313
CNT025 Central Pontine Myelinolysis 42 0.034
314
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 42 0.034
315
INT052 Intestinal Volvulus 42 0.034
316
NM001 Noma 42 0.034
317
HYP029 Hyperthyroxinemia 42 0.034
318
SYN053 Syndromic Diarrhea 42 0.034
319
BRN080 Brain Ischemia 41 0.034
320
c WLM002 Wilms Tumor 41 0.034
321
ESP023 Esophageal Disease 40 0.034
322
PRL008 Paralytic Ileus 39 0.034
323
P WLM008 Wilms Tumor, Type 1 39 0.034
324
RBF001 Riboflavin Deficiency 38 0.034
325
c BLN003 Blindness 37 0.034
326
PLR005 Pleuropneumonia 37 0.034
327
EMN001 Emanuel Syndrome 36 0.034
328
MCR094 Microvillus Inclusion Disease 35 0.034
329
FBR063 Fibrocalculous Pancreatic Diabetes 35 0.034
330
c HVY001 Heavy Chain Disease 35 0.034
331
AMN003 Amnestic Disorder 35 0.034
332
MTR001 Mature Cataract 34 0.034
333
ENM001 Enamel Caries 32 0.034
334
INT017 Intestinal Schistosomiasis 32 0.034
335
ARB001 Ariboflavinosis 32 0.034
336
P SLP004 Salpingo-Oophoritis 31 0.034
337
FLC001 Folic Acid Deficiency Anemia 30 0.034
338
ECT004 Ecthyma 30 0.034
339
PLT008 Pili Torti 29 0.034
340
PYR004 Pyuria 29 0.034
341
P ALP005 Alpha Chain Disease 29 0.034
342
BTN005 Biotin-Thiamine-Responsive Basal Ganglia Disease 28 0.034
343
MNT002 Mental Depression 28 0.034
344
CNG127 Congenital Sucrase-Isomaltase Deficiency 27 0.034
345
TNS007 Taeniasis 25 0.034
346
NTL001 Nut Allergic Reaction 22 0.034
347
P KRN003 Kernicterus Due to Isoimmunization 21 0.034
348
c BNG076 Benign Exophthalmos Syndrome 21 0.034
349
ANK010 Ankylostomiasis 20 0.034
350
BRL001 Brill-Zinsser Disease 19 0.034
351
P ISC010 Isochromosome Yp 14 0.034
352
HYP481 Hyperbiliverdinemia 14 0.034
353
INT050 Intestinal Impaction 14 0.034
354
HYP081 Hypolipoproteinemia 13 0.034
355
c HYP290 Hypobetalipoproteinemia, Familial, 2 8 0.034