Search results for "malnutrition"

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

282 hits were found for 'malnutrition'

# Family MCID Name MIFTS Score
1
PRT038 Protein-Energy Malnutrition 40 7.543
2
NTR005 Nutritional Deficiency Disease 28 2.741
3
KWS001 Kwashiorkor 41 0.223
4
PRT036 Peritonitis 61 0.166
5
P HPT021 Hepatitis 55 0.153
6
MRS001 Marasmus 40 0.149
7
P PNC044 Pancreatitis 59 0.129
8
XRP001 Xerophthalmia 31 0.123
9
P OBS005 Obesity 94 0.118
10
P DRR001 Diarrhea 44 0.118
11
ANR007 Anorexia Nervosa 62 0.112
12
INS024 Insulin-Like Growth Factor I 58 0.112
13
P THY032 Thyroiditis 56 0.112
14
MLR004 Malaria 81 0.105
15
LVR012 Liver Cirrhosis 66 0.105
16
ATH003 Atherosclerosis 56 0.105
17
ASC002 Ascariasis 39 0.105
18
CYS001 Cystic Fibrosis 92 0.098
19
ALC006 Alcoholic Hepatitis 58 0.098
20
URM002 Uremia 47 0.098
21
GRD001 Giardiasis 47 0.098
22
P PLL002 Pellagra 45 0.098
23
P LKM002 Leukemia 66 0.091
24
ISC004 Ischemia 53 0.091
25
TBR010 Tuberculosis 73 0.083
26
P ART022 Arthritis 65 0.083
27
MSL001 Measles 58 0.083
28
PRT019 Protein-Losing Enteropathy 47 0.083
29
MTB004 Metabolic Acidosis 38 0.083
30
CRB009 Cerebritis 33 0.083
31
TRP004 Tropical Sprue 30 0.083
32
P RHM011 Rheumatoid Arthritis 94 0.074
33
P RCK004 Rickets 58 0.074
34
P KDN018 Kidney Disease 57 0.074
35
c ACT073 Acute Leukemia 48 0.074
36
DYS073 Dysphagia 45 0.074
37
ANC001 Ancylostomiasis 36 0.074
38
P NRB001 Neuroblastoma 68 0.064
39
CRH001 Crohn's Disease 71 0.064
40
P LVR013 Liver Disease 62 0.064
41
P MNN013 Meningitis 58 0.064
42
P ESP024 Esophagitis 54 0.064
43
ETN001 Eating Disorder 49 0.064
44
MRB003 Morbid Obesity 52 0.064
45
P BLN003 Blindness 47 0.064
46
ACQ007 Acquired Immunodeficiency Syndrome 46 0.064
47
HYP037 Hyperhomocysteinemia 45 0.064
48
BRN080 Brain Ischemia 43 0.064
49
P NGH001 Night Blindness 42 0.064
50
DYS015 Dysentery 41 0.064
51
FDL002 Food Allergy 41 0.064
52
OVR063 Overnutrition 41 0.064
53
LCT002 Lactose Intolerance 40 0.064
54
BRB001 Beriberi 38 0.064
55
c ACT004 Acute Diarrhea 37 0.064
56
BTN004 Biotin Deficiency 35 0.064
57
HPT023 Hepatocellular Carcinoma 95 0.053
58
P LNG032 Lung Cancer 94 0.053
59
P DBT085 Diabetes Mellitus, Insulin-Dependent 83 0.053
60
P SCH015 Schizophrenia 79 0.053
61
P DLT002 Dilated Cardiomyopathy 77 0.053
62
HV1006 Hiv-1 83 0.053
63
CNG034 Congestive Heart Failure 69 0.053
64
P PNM007 Pneumonia 64 0.053
65
LSH001 Leishmaniasis 63 0.053
66
P WLM002 Wilms Tumor 70 0.053
67
SCH014 Schistosomiasis 60 0.053
68
c JVN010 Juvenile Rheumatoid Arthritis 59 0.053
69
P INF038 Influenza 67 0.053
70
c CHR089 Chronic Kidney Failure 57 0.053
71
END030 End Stage Renal Failure 56 0.053
72
P LYM026 Lymphoblastic Leukemia 55 0.053
73
GST009 Gastroschisis 55 0.053
74
c VRL010 Viral Hepatitis 54 0.053
75
DFC004 Deficiency Anemia 54 0.053
76
TTN003 Tetanus 54 0.053
77
GTR002 Goiter 53 0.053
78
P NRP001 Neuropathy 52 0.053
79
AMB001 Amebiasis 51 0.053
80
SCR002 Scurvy 51 0.053
81
VSC003 Visceral Leishmaniasis 50 0.053
82
TBR011 Tuberculous Meningitis 50 0.053
83
P CTR002 Cataract 50 0.053
84
BRN071 Brain Injury 49 0.053
85
P SDR002 Siderosis 49 0.053
86
PRC012 Pericardial Effusion 49 0.053
87
IRN001 Iron Deficiency Anemia 48 0.053
88
P HYP060 Hyperinsulinism 47 0.053
89
MCR094 Microvillus Inclusion Disease 44 0.053
90
ALC009 Alcoholic Liver Cirrhosis 43 0.053
91
PRT039 Proteinuria 43 0.053
92
VSC044 Visceral Myopathy 43 0.053
93
OBS001 Obstructive Jaundice 42 0.053
94
DNT012 Dental Caries 42 0.053
95
BRN106 Burns 42 0.053
96
KRT002 Keratomalacia 41 0.053
97
DNT001 Dental Fluorosis 41 0.053
98
P HYP058 Hypervitaminosis a 41 0.053
99
P CRB088 Cerebral Atrophy 40 0.053
100
P INF037 Inflammatory Bowel Disease 39 0.053
101
P TRC086 Trichohepatoenteric Syndrome 1 39 0.053
102
FTL021 Fetal Macrosomia 37 0.053
103
TRC023 Trichinosis 33 0.053
104
NCR001 Necrotizing Ulcerative Gingivitis 24 0.053
105
P CLR023 Colorectal Cancer 96 0.037
106
c SYS001 Systemic Lupus Erythematosus 91 0.037
107
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 82 0.037
108
P ATX030 Ataxia-Telangiectasia 76 0.037
109
GLC006 Galactosemia 75 0.037
110
P HMC003 Hemochromatosis 75 0.037
111
P OST002 Osteoporosis 71 0.037
112
SCK003 Sickle Cell Anemia 70 0.037
113
P CLC005 Celiac Disease 69 0.037
114
OBS002 Obsessive-Compulsive Disorder 69 0.037
115
ACR007 Acromegaly 69 0.037
116
P PRM002 Primary Hyperoxaluria 68 0.037
117
AND015 Androgen Insensitivity 69 0.037
118
P LPS004 Lupus Erythematosus 67 0.037
119
CHD001 Chediak-Higashi Syndrome 66 0.037
120
P NNN008 Noonan Syndrome 1 66 0.037
121
P ANG001 Angelman Syndrome 66 0.037
122
P CRD013 Cardiofaciocutaneous Syndrome 65 0.037
123
P THL005 Thalassemia 64 0.037
124
BLM001 Bloom Syndrome 64 0.037
125
P AMY004 Amyloidosis 63 0.037
126
P CNG401 Congenital Heart Disease 62 0.037
127
c HYP595 Hypertension, Essential 66 0.037
128
c HPT016 Hepatitis B 60 0.037
129
ALC007 Alcohol Dependence 60 0.037
130
OVR029 Ovarian Hyperstimulation Syndrome 60 0.037
131
P NPH012 Nephrotic Syndrome 60 0.037
132
RBS003 Rabson-Mendenhall Syndrome 60 0.037
133
LYS003 Lysinuric Protein Intolerance 60 0.037
134
P PRD008 Periodontitis 59 0.037
135
P PLY011 Polycystic Ovary Syndrome 59 0.037
136
VSC007 Vascular Disease 59 0.037
137
c MTB001 Metabolic Syndrome X 58 0.037
138
TRC008 Trachoma 58 0.037
139
c PRC016 Pre-Eclampsia 58 0.037
140
ART021 Arteriosclerosis 58 0.037
141
c HPT001 Hepatitis C 57 0.037
142
c LKM062 Leukemia, Acute Lymphoblastic 58 0.037
143
SHG001 Shigellosis 56 0.037
144
P GLL020 Gallbladder Disease 56 0.037
145
P OVR049 Ovarian Disease 56 0.037
146
OCL008 Oculopharyngeal Muscular Dystrophy 56 0.037
147
P ENC004 Encephalitis 56 0.037
148
STT001 Status Epilepticus 56 0.037
149
P HRD011 Hereditary Spherocytosis 56 0.037
150
CHL014 Cholera 56 0.037
151
BTN003 Biotinidase Deficiency 56 0.037
152
c VRL007 Viral Encephalitis 55 0.037
153
ACN002 Acanthosis Nigricans 55 0.037
154
P HYP076 Hyperthyroidism 54 0.037
155
CYS005 Cysticercosis 54 0.037
156
P FTL001 Fetal Alcohol Syndrome 54 0.037
157
P CND004 Candidiasis 54 0.037
158
CMP002 Campylobacteriosis 54 0.037
159
CHG001 Chagas Disease 54 0.037
160
P ACR001 Aicardi-Goutieres Syndrome 54 0.037
161
MYL020 Myelomeningocele 54 0.037
162
CRY003 Cryptosporidiosis 53 0.037
163
P ECL001 Eclampsia 53 0.037
164
TYP007 Typhoid Fever 53 0.037
165
HYP056 Hypoglycemia 53 0.037
166
P AND016 Andersen Syndrome 54 0.037
167
HYP066 Hyperglycemia 52 0.037
168
ADN001 Adenosine Deaminase Deficiency 52 0.037
169
STF001 Stiff-Person Syndrome 52 0.037
170
GNG013 Gingivitis 52 0.037
171
P FML012 Familial Partial Lipodystrophy 52 0.037
172
PLM001 Pulmonary Tuberculosis 60 0.037
173
MGC001 Megacolon 51 0.037
174
SCB001 Scabies 50 0.037
175
GLC003 Glucose Intolerance 50 0.037
176
BCT004 Bacteriuria 50 0.037
177
P INT068 Intestinal Disease 50 0.037
178
WHM001 Whim Syndrome 50 0.037
179
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.037
180
LPD010 Lipodystrophy 49 0.037
181
HYP266 Hypoxia 49 0.037
182
c CNT016 Central Retinal Vein Occlusion 49 0.037
183
BLM002 Bulimia Nervosa 49 0.037
184
P DGR001 Digeorge Syndrome 49 0.037
185
P MCR010 Microcephaly 49 0.037
186
VND002 Van Der Woude Syndrome 48 0.037
187
P RTN022 Retinal Vein Occlusion 48 0.037
188
ART001 Arterial Tortuosity Syndrome 48 0.037
189
CHY002 Chylomicron Retention Disease 48 0.037
190
c SPN225 Spondyloarthropathy 1 48 0.037
191
HMS001 Hemosiderosis 47 0.037
192
HYP077 Hypertrichosis 47 0.037
193
CRD005 Cardia Cancer 47 0.037
194
HYP458 Hyper Ige Syndrome 47 0.037
195
ACR005 Acrodermatitis 47 0.037
196
P HYP083 Hypopituitarism 47 0.037
197
PRM003 Premature Ejaculation 46 0.037
198
P SHR001 Short Bowel Syndrome 45 0.037
199
STT004 Steatorrhea 45 0.037
200
GST045 Gastroenteritis 45 0.037
201
THR013 Thoracic Outlet Syndrome 45 0.037
202
YLL001 Yellow Nail Syndrome 45 0.037
203
P MSC003 Muscular Atrophy 44 0.037
204
NM001 Noma 44 0.037
205
ESN005 Eosinophilic Gastroenteritis 44 0.037
206
c INT072 Intestinal Pseudo-Obstruction 44 0.037
207
END072 Endotheliitis 44 0.037
208
RTN023 Retinitis 44 0.037
209
P ALC004 Alcohol Abuse 48 0.037
210
PRP023 Peripheral Neuropathy 44 0.037
211
GLS007 Glossitis 43 0.037
212
P TCL004 T-Cell Leukemia 43 0.037
213
c CNG012 Congenital Generalized Lipodystrophy 43 0.037
214
URC002 Urea Cycle Disorder 43 0.037
215
LPD004 Lipoid Nephrosis 43 0.037
216
IMP004 Impetigo 43 0.037
217
P FRC002 Fructose Intolerance 44 0.037
218
ONC002 Onchocerciasis 43 0.037
219
ATX019 Ataxia with Vitamin E Deficiency 42 0.037
220
P CST002 Castleman's Disease 42 0.037
221
P NRV007 Nervous System Disease 42 0.037
222
MCR020 Microsporidiosis 42 0.037
223
c BCT007 Bacterial Meningitis 42 0.037
224
EXC002 Exocrine Pancreatic Insufficiency 41 0.037
225
LPD008 Lipid Metabolism Disorder 41 0.037
226
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 42 0.037
227
ALC010 Alcoholic Cardiomyopathy 41 0.037
228
P HYP345 Hyper-Ige Recurrent Infection Syndrome 42 0.037
229
P PNC001 Pancytopenia 41 0.037
230
c SVR005 Severe Pre-Eclampsia 40 0.037
231
c CNG415 Congenital Disorder of Glycosylation, Type Ia 40 0.037
232
FTT001 Fatty Liver Disease 39 0.037
233
TRN022 Transcobalamin Ii Deficiency 39 0.037
234
CNT025 Central Pontine Myelinolysis 39 0.037
235
BNF002 Bone Fracture 39 0.037
236
c MCL062 Mucolipidosis Ii Alpha/beta 39 0.037
237
MCR017 Macrocytic Anemia 38 0.037
238
AMN006 Aminoaciduria 37 0.037
239
PLC005 Placental Insufficiency 37 0.037
240
OLG010 Oligomenorrhea 37 0.037
241
HYP029 Hyperthyroxinemia 36 0.037
242
SNL007 Senile Cataract 36 0.037
243
WRN003 Wernicke Encephalopathy 35 0.037
244
SPR066 Superficial Siderosis 33 0.037
245
P HVY001 Heavy Chain Disease 33 0.037
246
c ART101 Aortic Valve Disease 2 32 0.037
247
PLT008 Pili Torti 32 0.037
248
IPX001 Ipex Syndrome 32 0.037
249
VRL011 Viral Infectious Disease 31 0.037
250
PSD029 Pseudocholinesterase Deficiency 31 0.037
251
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 30 0.037
252
PYR016 Pyridoxine Deficiency 30 0.037
253
ADS002 Adie Syndrome 30 0.037
254
NRT005 North Carolina Macular Dystrophy 29 0.037
255
P ATX010 Ataxia Neuropathy Spectrum 29 0.037
256
CLS040 Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 29 0.037
257
DYS070 Dysalbuminemic Hyperthyroxinemia 27 0.037
258
UND005 Undifferentiated Pleomorphic Sarcoma 28 0.037
259
TFT003 Tufting Enteropathy 26 0.037
260
c ALP060 Alpha Heavy-Chain Disease 26 0.037
261
HNM002 Hinman Syndrome 26 0.037
262
c CNG413 Congenital Short Bowel Syndrome 26 0.037
263
PYR004 Pyuria 24 0.037
264
SCR037 Sucrase-Isomaltase Deficiency, Congenital 24 0.037
265
TNS007 Taeniasis 23 0.037
266
ECT004 Ecthyma 22 0.037
267
MTC061 Mitochondrial Dna Depletion Syndrome 1 22 0.037
268
IRN002 Iron Metabolism Disease 22 0.037
269
HYP085 Hypothalamic Disease 23 0.037
270
THY039 Thyrotropin-Releasing Hormone Deficiency 21 0.037
271
OBS063 Obesity, Morbid, Due to Leptin Deficiency 20 0.037
272
BNT002 Bantu Siderosis 19 0.037
273
MNT002 Mental Depression 18 0.037
274
ATR073 Atrophic Glossitis 18 0.037
275
c BNG076 Benign Exophthalmos Syndrome 19 0.037
276
FML093 Familial Visceral Myopathy with External Ophthalmoplegia 18 0.037
277
EXC004 Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis 16 0.037
278
BRL001 Brill-Zinsser Disease 17 0.037
279
HYP481 Hyperbiliverdinemia 16 0.037
280
HYP081 Hypolipoproteinemia 16 0.037
281
MTC055 Mitochondrial Dna Depletion Syndrome 4b 13 0.037
282
c HYP290 Hypobetalipoproteinemia, Familial, 2 12 0.037