| Diseases | Rating | Bibliogr. | Expand |
---|
1 | Fetal Diseases | 100 | + + | |
2 | Goiter | 55 | + + | |
3 | Polyhydramnios | 10 | + + | |
4 | Abnormalities, Multiple | 10 | + + | |
5 | Fetal Growth Retardation | 9 | + + | |
6 | Prenatal Exposure Delayed Effects | 9 | + + | |
7 | Fetal Death | 8 | + + | |
8 | Trisomy | 7 | + + | |
9 | Syndrome | 6 | + + | |
10 | Hydrops Fetalis | 6 | + + | |
11 | Diseases in Twins | 6 | + + | |
12 | Holoprosencephaly | 5 | + + | |
13 | Chromosome Disorders | 5 | + + | |
14 | Chromosome Aberrations | 5 | + + | |
15 | Hernia, Umbilical | 4 | + + | |
16 | Congenital Abnormalities | 4 | + + | |
17 | Oligohydramnios | 4 | + + | |
18 | Lymphangioma, Cystic | 4 | + + | |
19 | Anencephaly | 4 | + + | |
20 | Twins, Conjoined | 4 | + + | |
21 | Aneuploidy | 4 | + + | |
22 | Arthrogryposis | 4 | + + | |
23 | Sex Chromosome Aberrations | 4 | + + | |
24 | Heart Defects, Congenital | 4 | + + | |
25 | Down Syndrome | 4 | + + | |
26 | Limb Deformities, Congenital | 3 | + + | |
27 | Craniofacial Abnormalities | 3 | + + | |
28 | Chromosome Deletion | 3 | + + | |
29 | Ectromelia | 3 | + + | |
30 | Prenatal Injuries | 3 | + + | |
31 | Teratoma | 3 | + + | |
32 | Thanatophoric Dysplasia | 3 | + + | |
33 | Pregnancy Complications | 3 | + + | |
34 | Osteochondrodysplasias | 3 | + + | |
35 | Hydrocolpos | 3 | + + | |
36 | Metabolism, Inborn Errors | 3 | + + | |
37 | Dandy-Walker Syndrome | 3 | + + | |
38 | Neural Tube Defects | 3 | + + | |
39 | Bone Diseases, Developmental | 3 | + + | |
40 | Acrocephalosyndactylia | 3 | + + | |
41 | Encephalocele | 3 | + + | |
42 | Clubfoot | 3 | + + | |
43 | Ichthyosis, Lamellar | 3 | + + | |
44 | Dwarfism | 3 | + + | |
45 | Urogenital Abnormalities | 3 | + + | |
46 | Hernia, Diaphragmatic | 2 | + + | |
47 | Monosomy | 2 | + + | |
48 | Genetic Diseases, Inborn | 2 | + + | |
49 | Meningomyelocele | 2 | + + | |
50 | Hydrocephalus | 2 | + + | |
51 | Placenta Diseases | 2 | + + | |
52 | Polydactyly | 2 | + + | |
53 | Intestinal Atresia | 2 | + + | |
54 | Osteogenesis Imperfecta | 2 | + + | |
55 | Amino Acid Metabolism, Inborn Errors | 2 | + + | |
56 | Maxillofacial Abnormalities | 2 | + + | |
57 | Isochromosomes | 2 | + + | |
58 | Achondroplasia | 2 | + + | |
59 | Polycystic Kidney Diseases | 2 | + + | |
60 | Agenesis of Corpus Callosum | 2 | + + | |
61 | Microcephaly | 2 | + + | |
62 | Ring Chromosomes | 2 | + + | |
63 | Translocation, Genetic | 2 | + + | |
64 | Anus, Imperforate | 2 | + + | |
65 | Toxoplasmosis, Congenital | 2 | + + | |
66 | Abortion, Spontaneous | 2 | + + | |
67 | Tetralogy of Fallot | 2 | + + | |
68 | Hydronephrosis | 2 | + + | |
69 | Cystic Adenomatoid Malformation of Lung, Congenital | 2 | + + | |
70 | Short Rib-Polydactyly Syndrome | 2 | + + | |
71 | Sex Chromosome Disorders | 2 | + + | |
72 | Sphingolipidoses | 2 | + + | |
73 | Abnormalities, Severe Teratoid | 2 | + + | |
74 | Nephroma, Mesoblastic | 2 | + + | |
75 | Chondrodysplasia Punctata | 2 | + + | |
76 | Ichthyosis | 2 | + + | |
77 | Hypophosphatasia | 2 | + + | |
78 | Cysts | 2 | + + | |
79 | Hyperargininemia | 2 | + + | |
80 | Asphyxia Neonatorum | 2 | + + | |
81 | Beckwith-Wiedemann Syndrome | 2 | + + | |
82 | Epidermolysis Bullosa | 2 | + + | |
83 | Micrognathism | 2 | + + | |
84 | Chromosome Inversion | 2 | + + | |
85 | Cleft Palate | 2 | + + | |
86 | Premature Birth | 2 | + + | |
87 | Ascites | 2 | + + | |
88 | Thalassemia | 1 | + + | |
89 | Prune Belly Syndrome | 1 | + + | |
90 | Epidermolysis Bullosa, Junctional | 1 | + + | |
91 | Gastroschisis | 1 | + + | |
92 | Adrenal Hyperplasia, Congenital | 1 | + + | |
93 | Obstetric Labor, Premature | 1 | + + | |
94 | Lymphangioma | 1 | + + | |
95 | Bladder Exstrophy | 1 | + + | |
96 | Spinal Dysraphism | 1 | + + | |
97 | Amniotic Band Syndrome | 1 | + + | |
98 | Fetal Weight | 1 | + + | |
99 | Mucolipidoses | 1 | + + | |
100 | Nervous System Malformations | 1 | + + | |
101 | Hypospadias | 1 | + + | |
102 | Mucopolysaccharidoses | 1 | + + | |
103 | Uniparental Disomy | 1 | + + | |
104 | Pregnancy Complications, Infectious | 1 | + + | |
105 | Abnormalities, Drug-Induced | 1 | + + | |
106 | Levocardia | 1 | + + | |
107 | Smith-Lemli-Opitz Syndrome | 1 | + + | |
108 | Hand Deformities, Congenital | 1 | + + | |
109 | Intellectual Disability | 1 | + + | |
110 | Muscular Dystrophies | 1 | + + | |
111 | Turner Syndrome | 1 | + + | |
112 | Mucopolysaccharidosis III | 1 | + + | |
113 | Birth Weight | 1 | + + | |
114 | beta-Thalassemia | 1 | + + | |
115 | Head and Neck Neoplasms | 1 | + + | |
116 | Urethral Obstruction | 1 | + + | |
117 | Klippel-Trenaunay-Weber Syndrome | 1 | + + | |
118 | Vein of Galen Malformations | 1 | + + | |
119 | Classical Lissencephalies and Subcortical Band Heterotopias | 1 | + + | |
120 | Malformations of Cortical Development | 1 | + + | |
121 | Lysosomal Storage Diseases | 1 | + + | |
122 | Lissencephaly | 1 | + + | |
123 | Rhabdomyoma | 1 | + + | |
124 | Cleft Lip | 1 | + + | |
125 | Cri-du-Chat Syndrome | 1 | + + | |
126 | Edema | 1 | + + | |
127 | alpha-Thalassemia | 1 | + + | |
128 | Infant, Premature, Diseases | 1 | + + | |
129 | Abnormal Karyotype | 1 | + + | |
130 | Myotonic Dystrophy | 1 | + + | |
131 | Skin Abnormalities | 1 | + + | |
132 | Facies | 1 | + + | |
133 | Infant, Newborn, Diseases | 1 | + + | |
134 | Pulmonary Atresia | 1 | + + | |
135 | Ellis-Van Creveld Syndrome | 1 | + + | |
136 | Spina Bifida Occulta | 1 | + + | |
137 | Ectodermal Dysplasia | 1 | + + | |
138 | Foot Deformities, Congenital | 1 | + + | |
139 | Disorders of Sex Development | 1 | + + | |
140 | Fetal Macrosomia | 1 | + + | |
141 | Hypertelorism | 1 | + + | |
142 | Sandhoff Disease | 1 | + + | |
143 | Tuberous Sclerosis | 1 | + + | |
144 | Nephrosis | 1 | + + | |
145 | Microphthalmos | 1 | + + | |
146 | Growth Disorders | 1 | + + | |
147 | Cystic Fibrosis | 1 | + + | |
148 | Chromosome Duplication | 1 | + + | |
149 | Craniosynostoses | 1 | + + | |
150 | Digestive System Abnormalities | 1 | + + | |
151 | Pierre Robin Syndrome | 1 | + + | |
152 | Goldenhar Syndrome | 1 | + + | |
153 | Eye Abnormalities | 1 | + + | |
154 | Lower Extremity Deformities, Congenital | 1 | + + | |
155 | Aortopulmonary Septal Defect | 1 | + + | |
156 | Hypoplastic Left Heart Syndrome | 1 | + + | |
157 | Hemangioma | 1 | + + | |
158 | Genetic Predisposition to Disease | 1 | + + | |
159 | Hydranencephaly | 1 | + + | |
160 | Fragile X Syndrome | 1 | + + | |
161 | Heart Septal Defects, Ventricular | 1 | + + | |
162 | Macroglossia | 1 | + + | |
163 | Citrullinemia | 1 | + + | |
164 | Brain Diseases | 1 | + + | |
165 | Dilatation, Pathologic | 1 | + + | |
166 | Genetic Diseases, X-Linked | 1 | + + | |
167 | Glycogen Storage Disease Type II | 1 | + + | |
168 | Rubella Syndrome, Congenital | 1 | + + | |
169 | Duodenal Obstruction | 1 | + + | |
170 | Pregnancy in Diabetics | 1 | + + | |
171 | Thoracic Diseases | 1 | + + | |
172 | Bronchopulmonary Sequestration | 1 | + + | |
173 | Leukomalacia, Periventricular | 1 | + + | |
174 | Muscle Hypertonia | 1 | + + | |
175 | Albinism, Oculocutaneous | 1 | + + | |
176 | Fanconi Anemia | 1 | + + | |
177 | Fetal Membranes, Premature Rupture | 1 | + + | |
178 | Spina Bifida Cystica | 1 | + + | |
179 | Neuronal Ceroid-Lipofuscinoses | 1 | + + | |
180 | Developmental Disabilities | 1 | + + | |
181 | Menkes Kinky Hair Syndrome | 1 | + + | |
182 | Choroideremia | 1 | + + | |
183 | Muscular Dystrophy, Duchenne | 1 | + + | |
184 | Cardiomegaly | 1 | + + | |
185 | Mucopolysaccharidosis II | 1 | + + | |
186 | Granulomatous Disease, Chronic | 1 | + + | |
187 | Cleidocranial Dysplasia | 1 | + + | |
188 | Diaphragmatic Eventration | 1 | + + | |
189 | Orofaciodigital Syndromes | 1 | + + | |
190 | Ectopia Cordis | 1 | + + | |
191 | Neuroblastoma | 1 | + + | |
192 | Septo-Optic Dysplasia | 1 | + + | |
193 | Polyploidy | 1 | + + | |
194 | DiGeorge Syndrome | 1 | + + | |
195 | Heart Septal Defects | 1 | + + | |
196 | Cardiovascular Abnormalities | 1 | + + | |
197 | Noonan Syndrome | 1 | + + | |
198 | Tay-Sachs Disease | 1 | + + | |
199 | Peroxisomal Disorders | 1 | + + | |
200 | De Lange Syndrome | 1 | + + | |
201 | Disease | 1 | + + | |
202 | Sjogren-Larsson Syndrome | 1 | + + | |
203 | Pentalogy of Cantrell | 1 | + + | |
204 | Hepatomegaly | 1 | + + | |
205 | Fetal Alcohol Spectrum Disorders | 1 | + + | |
206 | Hypohidrosis | 1 | + + | |
207 | Long QT Syndrome | 1 | + + | |
208 | Syndactyly | 1 | + + | |
209 | Carbohydrate Metabolism, Inborn Errors | 1 | + + | |
210 | Prader-Willi Syndrome | 1 | + + | |
211 | Huntington Disease | 1 | + + | |
212 | Tricuspid Atresia | 1 | + + | |
213 | Breech Presentation | 1 | + + | |
214 | Anophthalmos | 1 | + + | |
215 | Gangliosidoses | 1 | + + | |
216 | Ebstein Anomaly | 1 | + + | |
217 | Spinal Muscular Atrophies of Childhood | 1 | + + | |
218 | 46, XY Disorders of Sex Development | 1 | + + | |
219 | Eye Diseases, Hereditary | 1 | + + | |
220 | Collagen Diseases | 1 | + + | |