| Diseases | Rating | Bibliogr. | Expand |
---|
1 | Hypoxia, Brain | 100 | + + | |
2 | Anoxia | 98 | + + | |
3 | Fetal Hypoxia | 43 | + + | |
4 | Vitamin B 12 Deficiency | 15 | + + | |
5 | alpha 1-Antitrypsin Deficiency | 12 | + + | |
6 | Deficiency Diseases | 12 | + + | |
7 | IgA Deficiency | 12 | + + | |
8 | Asphyxia Neonatorum | 11 | + + | |
9 | Coma | 10 | + + | |
10 | Brain Damage, Chronic | 10 | + + | |
11 | Protein C Deficiency | 9 | + + | |
12 | Heart Arrest | 9 | + + | |
13 | Asphyxia | 9 | + + | |
14 | Myoclonus | 9 | + + | |
15 | Protein S Deficiency | 8 | + + | |
16 | Factor VII Deficiency | 7 | + + | |
17 | Immunologic Deficiency Syndromes | 7 | + + | |
18 | Vitamin A Deficiency | 7 | + + | |
19 | Metabolism, Inborn Errors | 7 | + + | |
20 | IgG Deficiency | 7 | + + | |
21 | Factor XI Deficiency | 6 | + + | |
22 | Vitamin D Deficiency | 6 | + + | |
23 | Factor X Deficiency | 6 | + + | |
24 | Folic Acid Deficiency | 6 | + + | |
25 | Antithrombin III Deficiency | 6 | + + | |
26 | Vitamin K Deficiency | 6 | + + | |
27 | Factor V Deficiency | 5 | + + | |
28 | Ornithine Carbamoyltransferase Deficiency Disease | 5 | + + | |
29 | Factor XIII Deficiency | 5 | + + | |
30 | Factor XII Deficiency | 5 | + + | |
31 | Thiamine Deficiency | 5 | + + | |
32 | Glucosephosphate Dehydrogenase Deficiency | 5 | + + | |
33 | Biotinidase Deficiency | 5 | + + | |
34 | Vitamin B Deficiency | 4 | + + | |
35 | Brain Diseases | 4 | + + | |
36 | Methemoglobinemia | 4 | + + | |
37 | Cyanosis | 4 | + + | |
38 | Vitamin E Deficiency | 4 | + + | |
39 | Carbon Monoxide Poisoning | 4 | + + | |
40 | Cytochrome-c Oxidase Deficiency | 4 | + + | |
41 | Altitude Sickness | 4 | + + | |
42 | Adrenal Hyperplasia, Congenital | 4 | + + | |
43 | Dysgammaglobulinemia | 4 | + + | |
44 | Anemia, Iron-Deficiency | 4 | + + | |
45 | Respiratory Insufficiency | 3 | + + | |
46 | Lecithin Acyltransferase Deficiency | 3 | + + | |
47 | Hypoxia-Ischemia, Brain | 3 | + + | |
48 | Protein Deficiency | 3 | + + | |
49 | Fructose-1,6-Diphosphatase Deficiency | 3 | + + | |
50 | Leukocyte-Adhesion Deficiency Syndrome | 3 | + + | |
51 | Vitamin B 6 Deficiency | 3 | + + | |
52 | Pulmonary Edema | 3 | + + | |
53 | Infant, Newborn, Diseases | 3 | + + | |
54 | Dihydropyrimidine Dehydrogenase Deficiency | 3 | + + | |
55 | Brain Diseases, Metabolic | 3 | + + | |
56 | Hypercapnia | 3 | + + | |
57 | Pyruvate Dehydrogenase Complex Deficiency Disease | 3 | + + | |
58 | Carbohydrate Metabolism, Inborn Errors | 3 | + + | |
59 | Syndrome | 3 | + + | |
60 | Hyperventilation | 2 | + + | |
61 | Lipid Metabolism, Inborn Errors | 2 | + + | |
62 | Ascorbic Acid Deficiency | 2 | + + | |
63 | Disease Models, Animal | 2 | + + | |
64 | Respiratory Distress Syndrome, Adult | 2 | + + | |
65 | Acidosis | 2 | + + | |
66 | Dwarfism, Pituitary | 2 | + + | |
67 | Acute Disease | 2 | + + | |
68 | Purine-Pyrimidine Metabolism, Inborn Errors | 2 | + + | |
69 | Anemia | 2 | + + | |
70 | Acidosis, Lactic | 2 | + + | |
71 | Metabolic Diseases | 2 | + + | |
72 | Necrosis | 2 | + + | |
73 | Dyspnea | 2 | + + | |
74 | Anemia, Hypochromic | 2 | + + | |
75 | Magnesium Deficiency | 2 | + + | |
76 | Pyruvate Carboxylase Deficiency Disease | 2 | + + | |
77 | Hyperoxia | 2 | + + | |
78 | Hepatopulmonary Syndrome | 2 | + + | |
79 | Sleep Apnea Syndromes | 2 | + + | |
80 | Decompression Sickness | 2 | + + | |
81 | Respiration Disorders | 2 | + + | |
82 | Embolism, Air | 2 | + + | |
83 | Apnea | 2 | + + | |
84 | Hemoglobinopathies | 2 | + + | |
85 | Recurrence | 2 | + + | |
86 | Pulmonary Embolism | 2 | + + | |
87 | Postoperative Complications | 2 | + + | |
88 | Muscular Diseases | 2 | + + | |
89 | Chronic Disease | 2 | + + | |
90 | Polycythemia | 2 | + + | |
91 | Growth Disorders | 2 | + + | |
92 | Acquired Immunodeficiency Syndrome | 2 | + + | |
93 | Respiratory Distress Syndrome, Newborn | 2 | + + | |
94 | Seizures | 2 | + + | |
95 | Hypertension, Pulmonary | 2 | + + | |
96 | Phenylketonurias | 2 | + + | |
97 | Airway Obstruction | 2 | + + | |
98 | Intraoperative Complications | 2 | + + | |
99 | Foramen Ovale, Patent | 2 | + + | |
100 | Mitochondrial Diseases | 2 | + + | |
101 | Hypoventilation | 1 | + + | |
102 | Hypoprothrombinemias | 1 | + + | |
103 | Anemia, Hemolytic | 1 | + + | |
104 | Hemorrhage | 1 | + + | |
105 | Multiple Carboxylase Deficiency | 1 | + + | |
106 | Hyperammonemia | 1 | + + | |
107 | Holocarboxylase Synthetase Deficiency | 1 | + + | |
108 | Muscle Hypotonia | 1 | + + | |
109 | Glycogen Storage Disease | 1 | + + | |
110 | Hyperargininemia | 1 | + + | |
111 | Genetic Predisposition to Disease | 1 | + + | |
112 | Malabsorption Syndromes | 1 | + + | |
113 | Pulmonary Disease, Chronic Obstructive | 1 | + + | |
114 | Critical Illness | 1 | + + | |
115 | Genetic Diseases, Inborn | 1 | + + | |
116 | Pregnancy Complications | 1 | + + | |
117 | Severe Combined Immunodeficiency | 1 | + + | |
118 | Brain Diseases, Metabolic, Inborn | 1 | + + | |
119 | Anemia, Hemolytic, Congenital Nonspherocytic | 1 | + + | |
120 | Lung Diseases | 1 | + + | |
121 | Hypoglycemia | 1 | + + | |
122 | Disease | 1 | + + | |
123 | Bronchopulmonary Dysplasia | 1 | + + | |
124 | Diseases in Twins | 1 | + + | |
125 | Anemia, Hemolytic, Congenital | 1 | + + | |
126 | Nervous System Diseases | 1 | + + | |
127 | Disorders of Sex Development | 1 | + + | |
128 | Mitochondrial Myopathies | 1 | + + | |
129 | Pregnancy Complications, Hematologic | 1 | + + | |
130 | Drowning | 1 | + + | |
131 | Agammaglobulinemia | 1 | + + | |
132 | Hypotension | 1 | + + | |
133 | Hypopituitarism | 1 | + + | |
134 | Anemia, Megaloblastic | 1 | + + | |
135 | Leigh Disease | 1 | + + | |
136 | Failure to Thrive | 1 | + + | |
137 | Alcoholism | 1 | + + | |
138 | Heart Septal Defects, Atrial | 1 | + + | |
139 | Lactose Intolerance | 1 | + + | |
140 | Anemia, Pernicious | 1 | + + | |
141 | Infant, Premature, Diseases | 1 | + + | |
142 | Vitamin K Deficiency Bleeding | 1 | + + | |
143 | Myoglobinuria | 1 | + + | |
144 | Rickets | 1 | + + | |
145 | Laryngismus | 1 | + + | |
146 | Sickle Cell Trait | 1 | + + | |
147 | Acidosis, Respiratory | 1 | + + | |
148 | Sleep Apnea, Central | 1 | + + | |
149 | Thrombophlebitis | 1 | + + | |
150 | Pneumonia | 1 | + + | |
151 | Anemia, Sickle Cell | 1 | + + | |
152 | Hypolipoproteinemias | 1 | + + | |
153 | Adrenal Insufficiency | 1 | + + | |
154 | Homocystinuria | 1 | + + | |
155 | Glycogen Storage Disease Type VII | 1 | + + | |
156 | Multiple Acyl Coenzyme A Dehydrogenase Deficiency | 1 | + + | |
157 | Pulmonary Emphysema | 1 | + + | |
158 | Infant Nutrition Disorders | 1 | + + | |
159 | Anemia, Macrocytic | 1 | + + | |
160 | Osteoradionecrosis | 1 | + + | |
161 | Obesity | 1 | + + | |
162 | Brain Injuries | 1 | + + | |
163 | Angioedema | 1 | + + | |
164 | Developmental Disabilities | 1 | + + | |
165 | Hyperlipoproteinemia Type I | 1 | + + | |
166 | Bradycardia | 1 | + + | |
167 | Ataxia | 1 | + + | |
168 | Carbamoyl-Phosphate Synthase I Deficiency Disease | 1 | + + | |
169 | Sclerema Neonatorum | 1 | + + | |
170 | Wounds and Injuries | 1 | + + | |
171 | Intellectual Disability | 1 | + + | |
172 | Near Drowning | 1 | + + | |
173 | Heart Defects, Congenital | 1 | + + | |
174 | Metal Metabolism, Inborn Errors | 1 | + + | |
175 | Thrombosis | 1 | + + | |
176 | Brain Ischemia | 1 | + + | |
177 | Lymphopenia | 1 | + + | |
178 | Disease Susceptibility | 1 | + + | |
179 | Lung Injury | 1 | + + | |
180 | Hemolysis | 1 | + + | |
181 | Psychomotor Disorders | 1 | + + | |
182 | Craniocerebral Trauma | 1 | + + | |
183 | Ketosis | 1 | + + | |
184 | Respiratory Tract Infections | 1 | + + | |
185 | Steroid Metabolism, Inborn Errors | 1 | + + | |
186 | Ischemia | 1 | + + | |
187 | Shock | 1 | + + | |
188 | Hemophilia A | 1 | + + | |
189 | Brain Edema | 1 | + + | |
190 | Fetal Diseases | 1 | + + | |
191 | Decerebrate State | 1 | + + | |
192 | Lung Diseases, Obstructive | 1 | + + | |
193 | Tetralogy of Fallot | 1 | + + | |
194 | Persistent Fetal Circulation Syndrome | 1 | + + | |
195 | Fetal Distress | 1 | + + | |
196 | Hemorrhagic Disorders | 1 | + + | |
197 | Fetal Death | 1 | + + | |
198 | Barotrauma | 1 | + + | |
199 | Hypogonadism | 1 | + + | |
200 | Hypothyroidism | 1 | + + | |
201 | Radiation Injuries | 1 | + + | |
202 | Asthma | 1 | + + | |
203 | Infection | 1 | + + | |
204 | Coagulation Protein Disorders | 1 | + + | |
205 | Leg Ulcer | 1 | + + | |
206 | Thrombophilia | 1 | + + | |
207 | Hemophilia B | 1 | + + | |
208 | Eisenmenger Complex | 1 | + + | |
209 | Abnormalities, Multiple | 1 | + + | |
210 | Hypertension | 1 | + + | |
211 | Cardiomegaly | 1 | + + | |
212 | Neuromuscular Diseases | 1 | + + | |
213 | Cerebral Hemorrhage | 1 | + + | |
214 | Lesch-Nyhan Syndrome | 1 | + + | |
215 | Paraphilias | 1 | + + | |
216 | Sudden Infant Death | 1 | + + | |
217 | Spherocytosis, Hereditary | 1 | + + | |
218 | Thromboembolism | 1 | + + | |
219 | Acrodermatitis | 1 | + + | |
220 | Riboflavin Deficiency | 1 | + + | |
221 | Pulmonary Fibrosis | 1 | + + | |
222 | Xerophthalmia | 1 | + + | |
223 | Epilepsy | 1 | + + | |
224 | Leukodystrophy, Metachromatic | 1 | + + | |
225 | Glycogen Storage Disease Type V | 1 | + + | |
226 | Avitaminosis | 1 | + + | |
227 | Glycogen Storage Disease Type II | 1 | + + | |
228 | Bacterial Infections | 1 | + + | |
229 | Mevalonate Kinase Deficiency | 1 | + + | |
230 | Liver Cirrhosis | 1 | + + | |
231 | Reperfusion Injury | 1 | + + | |
232 | Cardiomyopathies | 1 | + + | |
233 | Frostbite | 1 | + + | |
234 | Jaundice, Neonatal | 1 | + + | |
235 | Muscle Cramp | 1 | + + | |
236 | Hepatomegaly | 1 | + + | |
237 | Prolidase Deficiency | 1 | + + | |