| Diseases | Rating | Bibliogr. | Expand |
---|
1 | Vitamin B 12 Deficiency | 100 | + + | |
2 | Vitamin A Deficiency | 68 | + + | |
3 | Vitamin D Deficiency | 57 | + + | |
4 | Vitamin K Deficiency | 50 | + + | |
5 | Vitamin E Deficiency | 37 | + + | |
6 | Deficiency Diseases | 24 | + + | |
7 | alpha 1-Antitrypsin Deficiency | 23 | + + | |
8 | IgA Deficiency | 23 | + + | |
9 | Protein C Deficiency | 19 | + + | |
10 | Vitamin K Deficiency Bleeding | 19 | + + | |
11 | Vitamin B 6 Deficiency | 18 | + + | |
12 | Protein S Deficiency | 16 | + + | |
13 | Rickets | 16 | + + | |
14 | Folic Acid Deficiency | 16 | + + | |
15 | Factor VII Deficiency | 15 | + + | |
16 | Metabolism, Inborn Errors | 15 | + + | |
17 | Hypervitaminosis A | 14 | + + | |
18 | Immunologic Deficiency Syndromes | 14 | + + | |
19 | Malabsorption Syndromes | 13 | + + | |
20 | Factor X Deficiency | 13 | + + | |
21 | IgG Deficiency | 13 | + + | |
22 | Factor XI Deficiency | 12 | + + | |
23 | Antithrombin III Deficiency | 11 | + + | |
24 | Factor V Deficiency | 11 | + + | |
25 | Ornithine Carbamoyltransferase Deficiency Disease | 10 | + + | |
26 | Factor XIII Deficiency | 10 | + + | |
27 | Factor XII Deficiency | 10 | + + | |
28 | Thiamine Deficiency | 10 | + + | |
29 | Anemia, Megaloblastic | 10 | + + | |
30 | Glucosephosphate Dehydrogenase Deficiency | 10 | + + | |
31 | Vitamin B Deficiency | 9 | + + | |
32 | Biotinidase Deficiency | 9 | + + | |
33 | Anemia, Iron-Deficiency | 9 | + + | |
34 | Xerophthalmia | 9 | + + | |
35 | Protein Deficiency | 8 | + + | |
36 | Anemia, Macrocytic | 8 | + + | |
37 | Cytochrome-c Oxidase Deficiency | 8 | + + | |
38 | Adrenal Hyperplasia, Congenital | 7 | + + | |
39 | Dysgammaglobulinemia | 7 | + + | |
40 | Osteomalacia | 7 | + + | |
41 | Hypocalcemia | 7 | + + | |
42 | Hypoprothrombinemias | 7 | + + | |
43 | Avitaminosis | 7 | + + | |
44 | Lecithin Acyltransferase Deficiency | 7 | + + | |
45 | Fructose-1,6-Diphosphatase Deficiency | 6 | + + | |
46 | Leukocyte-Adhesion Deficiency Syndrome | 6 | + + | |
47 | Dihydropyrimidine Dehydrogenase Deficiency | 6 | + + | |
48 | Night Blindness | 6 | + + | |
49 | Abetalipoproteinemia | 5 | + + | |
50 | Pyruvate Dehydrogenase Complex Deficiency Disease | 5 | + + | |
51 | Carbohydrate Metabolism, Inborn Errors | 5 | + + | |
52 | Familial Hypophosphatemic Rickets | 5 | + + | |
53 | Magnesium Deficiency | 5 | + + | |
54 | Lipid Metabolism, Inborn Errors | 5 | + + | |
55 | Metabolic Diseases | 5 | + + | |
56 | Anemia, Hypochromic | 5 | + + | |
57 | Ascorbic Acid Deficiency | 5 | + + | |
58 | Coagulation Protein Disorders | 5 | + + | |
59 | Nervous System Diseases | 5 | + + | |
60 | Homocystinuria | 5 | + + | |
61 | Dwarfism, Pituitary | 5 | + + | |
62 | Syndrome | 5 | + + | |
63 | Brain Diseases, Metabolic | 4 | + + | |
64 | Purine-Pyrimidine Metabolism, Inborn Errors | 4 | + + | |
65 | Ataxia | 4 | + + | |
66 | Muscular Diseases | 4 | + + | |
67 | Failure to Thrive | 4 | + + | |
68 | Hyperhomocysteinemia | 4 | + + | |
69 | Hypercalcemia | 4 | + + | |
70 | Pyruvate Carboxylase Deficiency Disease | 4 | + + | |
71 | Nutrition Disorders | 4 | + + | |
72 | Hypoparathyroidism | 4 | + + | |
73 | Subacute Combined Degeneration | 4 | + + | |
74 | Hyperparathyroidism, Secondary | 4 | + + | |
75 | Growth Disorders | 4 | + + | |
76 | Muscle Hypotonia | 4 | + + | |
77 | Phenylketonurias | 4 | + + | |
78 | Genetic Predisposition to Disease | 4 | + + | |
79 | Acquired Immunodeficiency Syndrome | 4 | + + | |
80 | Recurrence | 3 | + + | |
81 | Acidosis | 3 | + + | |
82 | Anemia, Hemolytic | 3 | + + | |
83 | Celiac Disease | 3 | + + | |
84 | Multiple Carboxylase Deficiency | 3 | + + | |
85 | Hyperammonemia | 3 | + + | |
86 | Holocarboxylase Synthetase Deficiency | 3 | + + | |
87 | Glycogen Storage Disease | 3 | + + | |
88 | Pregnancy Complications | 3 | + + | |
89 | Hyperargininemia | 3 | + + | |
90 | Mitochondrial Diseases | 3 | + + | |
91 | Wernicke Encephalopathy | 3 | + + | |
92 | Genetic Diseases, Inborn | 3 | + + | |
93 | Severe Combined Immunodeficiency | 3 | + + | |
94 | Hemorrhagic Disorders | 3 | + + | |
95 | Alopecia | 3 | + + | |
96 | Spinal Cord Diseases | 3 | + + | |
97 | Brain Diseases, Metabolic, Inborn | 3 | + + | |
98 | Anemia, Hemolytic, Congenital Nonspherocytic | 3 | + + | |
99 | Acidosis, Lactic | 3 | + + | |
100 | Peripheral Nervous System Diseases | 3 | + + | |
101 | Pregnancy Complications, Hematologic | 3 | + + | |
102 | Malnutrition | 3 | + + | |
103 | Disease | 3 | + + | |
104 | Anemia | 3 | + + | |
105 | Developmental Disabilities | 3 | + + | |
106 | Disease Susceptibility | 3 | + + | |
107 | Osteoporosis | 3 | + + | |
108 | Bone Diseases, Metabolic | 3 | + + | |
109 | Hemorrhage | 3 | + + | |
110 | Seizures | 3 | + + | |
111 | Blood Coagulation Disorders | 3 | + + | |
112 | Cystic Fibrosis | 3 | + + | |
113 | Hemophilia B | 3 | + + | |
114 | Thrombophlebitis | 3 | + + | |
115 | Disorders of Sex Development | 3 | + + | |
116 | Infant, Newborn, Diseases | 3 | + + | |
117 | Agammaglobulinemia | 3 | + + | |
118 | Pseudohypoparathyroidism | 2 | + + | |
119 | Riboflavin Deficiency | 2 | + + | |
120 | Neuromuscular Diseases | 2 | + + | |
121 | Hypopituitarism | 2 | + + | |
122 | Hypercalciuria | 2 | + + | |
123 | Anemia, Hemolytic, Congenital | 2 | + + | |
124 | Hypophosphatemia | 2 | + + | |
125 | Leigh Disease | 2 | + + | |
126 | Lactose Intolerance | 2 | + + | |
127 | Anemia, Pernicious | 2 | + + | |
128 | Myoglobinuria | 2 | + + | |
129 | Pancytopenia | 2 | + + | |
130 | Pellagra | 2 | + + | |
131 | Short Bowel Syndrome | 2 | + + | |
132 | Intellectual Disability | 2 | + + | |
133 | Chronic Disease | 2 | + + | |
134 | Obesity, Morbid | 2 | + + | |
135 | Beriberi | 2 | + + | |
136 | Hypolipoproteinemias | 2 | + + | |
137 | Psychomotor Disorders | 2 | + + | |
138 | Adrenal Insufficiency | 2 | + + | |
139 | Atrophy | 2 | + + | |
140 | Alcoholism | 2 | + + | |
141 | Glycogen Storage Disease Type VII | 2 | + + | |
142 | Multiple Acyl Coenzyme A Dehydrogenase Deficiency | 2 | + + | |
143 | Muscle Weakness | 2 | + + | |
144 | Infant Nutrition Disorders | 2 | + + | |
145 | Angioedema | 2 | + + | |
146 | Mitochondrial Myopathies | 2 | + + | |
147 | Hypothyroidism | 2 | + + | |
148 | Blood Coagulation Disorders, Inherited | 2 | + + | |
149 | Hyperlipoproteinemia Type I | 2 | + + | |
150 | Cerebellar Ataxia | 2 | + + | |
151 | Thrombosis | 2 | + + | |
152 | Carbamoyl-Phosphate Synthase I Deficiency Disease | 2 | + + | |
153 | Glycogen Storage Disease Type V | 2 | + + | |
154 | Thrombophilia | 2 | + + | |
155 | Metal Metabolism, Inborn Errors | 2 | + + | |
156 | Epilepsy | 2 | + + | |
157 | Intracranial Hemorrhages | 2 | + + | |
158 | Hypoglycemia | 2 | + + | |
159 | Lymphopenia | 2 | + + | |
160 | Child Nutrition Disorders | 2 | + + | |
161 | Obesity | 2 | + + | |
162 | Ketosis | 2 | + + | |
163 | Steroid Metabolism, Inborn Errors | 2 | + + | |
164 | Thromboembolism | 2 | + + | |
165 | Hemolysis | 2 | + + | |
166 | Hemophilia A | 2 | + + | |
167 | Glossitis | 2 | + + | |
168 | Liver Cirrhosis | 2 | + + | |
169 | Jaundice, Neonatal | 2 | + + | |
170 | Hepatomegaly | 2 | + + | |
171 | Hypogonadism | 2 | + + | |
172 | Diseases in Twins | 2 | + + | |
173 | Abnormalities, Multiple | 2 | + + | |
174 | Eczema | 2 | + + | |
175 | Respiratory Tract Infections | 2 | + + | |
176 | Nephrolithiasis | 2 | + + | |
177 | Lesch-Nyhan Syndrome | 2 | + + | |
178 | Skin Diseases | 2 | + + | |
179 | Brain Diseases | 2 | + + | |
180 | Spherocytosis, Hereditary | 2 | + + | |
181 | Fatigue | 2 | + + | |
182 | Nephrocalcinosis | 2 | + + | |
183 | Acrodermatitis | 2 | + + | |
184 | Calcinosis | 2 | + + | |
185 | Friedreich Ataxia | 2 | + + | |
186 | Pallor | 2 | + + | |
187 | Leukodystrophy, Metachromatic | 2 | + + | |
188 | Liver Diseases | 2 | + + | |
189 | Diarrhea | 2 | + + | |
190 | Hemarthrosis | 2 | + + | |
191 | Kidney Failure, Chronic | 1 | + + | |
192 | Infection | 1 | + + | |
193 | Intestinal Diseases | 1 | + + | |
194 | Glycogen Storage Disease Type II | 1 | + + | |
195 | Protein-Energy Malnutrition | 1 | + + | |
196 | Mevalonate Kinase Deficiency | 1 | + + | |
197 | Ecchymosis | 1 | + + | |
198 | Hyperparathyroidism | 1 | + + | |
199 | Achlorhydria | 1 | + + | |
200 | Fanconi Syndrome | 1 | + + | |
201 | Blood Platelet Disorders | 1 | + + | |
202 | Body Weight | 1 | + + | |
203 | Muscle Cramp | 1 | + + | |
204 | Disease Progression | 1 | + + | |
205 | Paresthesia | 1 | + + | |
206 | Prolidase Deficiency | 1 | + + | |
207 | Ichthyosis | 1 | + + | |
208 | Vomiting | 1 | + + | |
209 | Prenatal Exposure Delayed Effects | 1 | + + | |
210 | Peroxisomal Disorders | 1 | + + | |
211 | Galactosemias | 1 | + + | |
212 | Common Variable Immunodeficiency | 1 | + + | |
213 | Cerebral Hemorrhage | 1 | + + | |
214 | Postoperative Complications | 1 | + + | |
215 | Pyruvate Metabolism, Inborn Errors | 1 | + + | |
216 | Purpura | 1 | + + | |
217 | Hypobetalipoproteinemias | 1 | + + | |
218 | Vaginitis | 1 | + + | |
219 | Acute Disease | 1 | + + | |
220 | Blood Protein Disorders | 1 | + + | |
221 | Polyneuropathies | 1 | + + | |
222 | Kwashiorkor | 1 | + + | |
223 | Movement Disorders | 1 | + + | |
224 | Citrullinemia | 1 | + + | |
225 | Genetic Diseases, X-Linked | 1 | + + | |
226 | Disease Models, Animal | 1 | + + | |
227 | Coma | 1 | + + | |
228 | Infant, Premature, Diseases | 1 | + + | |
229 | Corneal Opacity | 1 | + + | |
230 | Proteinuria | 1 | + + | |
231 | Abnormalities, Drug-Induced | 1 | + + | |
232 | Venous Thrombosis | 1 | + + | |
233 | Postgastrectomy Syndromes | 1 | + + | |
234 | Cholestasis | 1 | + + | |
235 | Spinocerebellar Degenerations | 1 | + + | |
236 | Neurologic Manifestations | 1 | + + | |
237 | Cardiomyopathies | 1 | + + | |
238 | Mitochondrial Encephalomyopathies | 1 | + + | |
239 | Hyperemesis Gravidarum | 1 | + + | |
240 | Bronchiectasis | 1 | + + | |
241 | Cholestasis, Intrahepatic | 1 | + + | |
242 | Autoimmune Diseases | 1 | + + | |
243 | Mucopolysaccharidoses | 1 | + + | |
244 | Hand Deformities | 1 | + + | |
245 | Reye Syndrome | 1 | + + | |
246 | Osteitis Fibrosa Cystica | 1 | + + | |
247 | Feeding and Eating Disorders of Childhood | 1 | + + | |
248 | Hypoaldosteronism | 1 | + + | |
249 | Pulmonary Emphysema | 1 | + + | |
250 | Necrosis | 1 | + + | |
251 | Hyperlipoproteinemias | 1 | + + | |
252 | Endocrine System Diseases | 1 | + + | |
253 | Erythema | 1 | + + | |
254 | Rhabdomyolysis | 1 | + + | |
255 | Scurvy | 1 | + + | |
256 | Bronchopneumonia | 1 | + + | |
257 | Glycosuria | 1 | + + | |
258 | Hypophosphatasia | 1 | + + | |
259 | Methemoglobinemia | 1 | + + | |
260 | Meningitis, Meningococcal | 1 | + + | |
261 | Spasms, Infantile | 1 | + + | |
262 | Muscular Dystrophies | 1 | + + | |
263 | Lysosomal Storage Diseases | 1 | + + | |
264 | Gangliosidoses | 1 | + + | |
265 | Fetal Diseases | 1 | + + | |
266 | Tetany | 1 | + + | |
267 | Puberty, Delayed | 1 | + + | |
268 | Sphingolipidoses | 1 | + + | |
269 | Exocrine Pancreatic Insufficiency | 1 | + + | |
270 | Drug Overdose | 1 | + + | |
271 | Liver Diseases, Alcoholic | 1 | + + | |
272 | Bacterial Infections | 1 | + + | |
273 | Hyperbilirubinemia | 1 | + + | |
274 | Dent Disease | 1 | + + | |
275 | Osteoporosis, Postmenopausal | 1 | + + | |
276 | Hyperlipidemias | 1 | + + | |
277 | Hypoproteinemia | 1 | + + | |
278 | Pica | 1 | + + | |
279 | Hematologic Diseases | 1 | + + | |
280 | Skin Diseases, Metabolic | 1 | + + | |
281 | Pain | 1 | + + | |
282 | 46, XX Disorders of Sex Development | 1 | + + | |
283 | Osteopetrosis | 1 | + + | |
284 | Lupus Erythematosus, Systemic | 1 | + + | |
285 | Sensation Disorders | 1 | + + | |
286 | Menorrhagia | 1 | + + | |
287 | Fatty Liver | 1 | + + | |
288 | Nerve Degeneration | 1 | + + | |
289 | Amenorrhea | 1 | + + | |
290 | Acne Vulgaris | 1 | + + | |
291 | Mucopolysaccharidosis I | 1 | + + | |
292 | Anorexia | 1 | + + | |
293 | Corneal Diseases | 1 | + + | |
294 | Bone Resorption | 1 | + + | |
295 | Psychotic Disorders | 1 | + + | |
296 | Blood Loss, Surgical | 1 | + + | |
297 | Blind Loop Syndrome | 1 | + + | |
298 | Dry Eye Syndromes | 1 | + + | |
299 | Favism | 1 | + + | |
300 | Cerebellar Diseases | 1 | + + | |
301 | Conjunctivitis | 1 | + + | |
302 | Tangier Disease | 1 | + + | |
303 | Weight Loss | 1 | + + | |
304 | Crohn Disease | 1 | + + | |
305 | Congenital Disorders of Glycosylation | 1 | + + | |
306 | Eating Disorders | 1 | + + | |
307 | Fractures, Spontaneous | 1 | + + | |
308 | Reflex, Abnormal | 1 | + + | |
309 | Drug Eruptions | 1 | + + | |
310 | Pigmentation Disorders | 1 | + + | |
311 | Muscular Atrophy | 1 | + + | |
312 | Renal Osteodystrophy | 1 | + + | |
313 | Fabry Disease | 1 | + + | |
314 | Acute Kidney Injury | 1 | + + | |
315 | Chondrodysplasia Punctata | 1 | + + | |
316 | Retinitis Pigmentosa | 1 | + + | |
317 | Eye Manifestations | 1 | + + | |
318 | Liver Cirrhosis, Biliary | 1 | + + | |
319 | Ichthyosis, X-Linked | 1 | + + | |
320 | Lipidoses | 1 | + + | |
321 | Cardiomyopathy, Dilated | 1 | + + | |
322 | Sepsis | 1 | + + | |
323 | Hypertension | 1 | + + | |
324 | Hyperphosphatemia | 1 | + + | |
325 | Hyperoxaluria | 1 | + + | |
326 | Diabetes Mellitus, Type 1 | 1 | + + | |
327 | Dystonia | 1 | + + | |
328 | Steatorrhea | 1 | + + | |
329 | alpha-Mannosidosis | 1 | + + | |
330 | Mucopolysaccharidosis IV | 1 | + + | |
331 | Tooth Diseases | 1 | + + | |
332 | Mobility Limitation | 1 | + + | |
333 | Delirium, Dementia, Amnestic, Cognitive Disorders | 1 | + + | |
334 | Multiple Sulfatase Deficiency Disease | 1 | + + | |
335 | Urea Cycle Disorders, Inborn | 1 | + + | |
336 | Substance-Related Disorders | 1 | + + | |
337 | Chromosome Deletion | 1 | + + | |
338 | Mucolipidoses | 1 | + + | |
339 | Epistaxis | 1 | + + | |
340 | Dehydration | 1 | + + | |
341 | Neurodegenerative Diseases | 1 | + + | |
342 | Renal Insufficiency | 1 | + + | |
343 | Giardiasis | 1 | + + | |
344 | Dwarfism | 1 | + + | |
345 | Neutropenia | 1 | + + | |
346 | Gingival Hemorrhage | 1 | + + | |
347 | Leukopenia | 1 | + + | |
348 | Renal Aminoacidurias | 1 | + + | |
349 | Disseminated Intravascular Coagulation | 1 | + + | |
350 | Central Nervous System Diseases | 1 | + + | |
351 | Diabetes Mellitus, Type 2 | 1 | + + | |
352 | Pityriasis Rubra Pilaris | 1 | + + | |
353 | Hypertriglyceridemia | 1 | + + | |
354 | Gaucher Disease | 1 | + + | |
355 | Renal Insufficiency, Chronic | 1 | + + | |
356 | Basal Ganglia Diseases | 1 | + + | |
357 | Meningococcal Infections | 1 | + + | |
358 | Demyelinating Diseases | 1 | + + | |
359 | Pulmonary Embolism | 1 | + + | |
360 | Respiratory Insufficiency | 1 | + + | |
361 | Bone Diseases | 1 | + + | |
362 | Lung Diseases | 1 | + + | |
363 | Glossalgia | 1 | + + | |
364 | Sarcoma, Kaposi | 1 | + + | |
365 | Dermatitis | 1 | + + | |
366 | Oral Hemorrhage | 1 | + + | |
367 | Cystinuria | 1 | + + | |
368 | Urinary Calculi | 1 | + + | |
369 | Microcephaly | 1 | + + | |
370 | Leukoencephalopathies | 1 | + + | |
371 | beta-Thalassemia | 1 | + + | |
372 | Myoclonus | 1 | + + | |
373 | Congenital Hypothyroidism | 1 | + + | |
374 | Hyperpigmentation | 1 | + + | |
375 | Monckeberg Medial Calcific Sclerosis | 1 | + + | |
376 | Thrombocytopenia | 1 | + + | |
377 | Kidney Diseases | 1 | + + | |
378 | Amino Acid Metabolism, Inborn Errors | 1 | + + | |
379 | Neoplasms | 1 | + + | |
380 | Myasthenic Syndromes, Congenital | 1 | + + | |
381 | Autistic Disorder | 1 | + + | |
382 | Keratosis | 1 | + + | |
383 | Mycobacterium Infections | 1 | + + | |
384 | Diarrhea, Infantile | 1 | + + | |
385 | Hirsutism | 1 | + + | |
386 | Cardiovascular Diseases | 1 | + + | |
387 | Granulomatous Disease, Chronic | 1 | + + | |
388 | Tay-Sachs Disease | 1 | + + | |
389 | Cytomegalovirus Infections | 1 | + + | |
390 | Dyskinesias | 1 | + + | |
391 | Hyaline Membrane Disease | 1 | + + | |
392 | Ectromelia | 1 | + + | |
393 | Skin Manifestations | 1 | + + | |
394 | Puberty, Precocious | 1 | + + | |
395 | Vision Disorders | 1 | + + | |
396 | Sandhoff Disease | 1 | + + | |
397 | Bone Marrow Diseases | 1 | + + | |
398 | Respiratory Distress Syndrome, Newborn | 1 | + + | |
399 | Antley-Bixler Syndrome Phenotype | 1 | + + | |
400 | Lymphangiectasis, Intestinal | 1 | + + | |
401 | Immune System Diseases | 1 | + + | |
402 | Venous Thromboembolism | 1 | + + | |
403 | Musculoskeletal Pain | 1 | + + | |