Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Supernumerary ear lobule |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Brachymetapody |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Phosphatidylcholine-sterol acyltransferase deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
1 |
Juvenile type megaloblastic anemia |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
Umbilical hernia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Immature fetus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
diastématomyélie |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Congenital anomaly of retina |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Non-fluoride enamel opacities |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Microgyria |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Ectopic adrenal gland (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Double ureter |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital atresia of ureter |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Severe combined immunodeficiency due to absent T cell receptor (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
Adult chronic GM2 gangliosidosis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Congenital anomaly of gallbladder |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Succinate-semialdehyde dehydrogenase deficiency (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Bilateral congenital macrostomia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Disto-occlusion of teeth |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Podencephalus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Ectopic fetus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Familial lipoprotein deficiency (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
FG syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Lysinuric protein intolerance, type 1 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Osteochondrodysplasia with osteopetrosis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Beals auriculo-osteodysplasia syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Kernicterus of newborn |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital enlargement of nasopharynx |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Funnel-shaped pelvis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital stenosis of aqueduct of Sylvius |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Complete unilateral cleft palate with cleft lip |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Anomaly of chromosome pair 9 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital atresia of bronchus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Fordyce's disease |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Testosterone 17-beta-dehydrogenase deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
A sex chromosome aneuploidy where males receive an additional Y chromosome, and with clinical characteristics of tall stature evident from childhood, macrocephaly, facial features (mild hypertelorism, low set ears, a mildly flat malar region), speech delay and an increased risk for social and emotional difficulties, attention deficit hyperactive disorder and autistic spectrum disorder. |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Sinus pericranii |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Accessory skeletal muscle |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Periodontal Ehlers-Danlos syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Brachypellic pelvis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Ectopic testis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Grob's syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital anomaly of bronchus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Accessory nipple (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Gangliosidosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Congenital fistula of urachus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
22q partial trisomy (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital organoaxial volvulus of stomach (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Leukodystrophy |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Agenesis of corpus callosum |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Erythropoietic protoporphyria |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Congenital obstruction of bile duct |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Diprosopus tetrophthalmus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital constriction of pylorus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Birthmark |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Transient neonatal hyperglycinemia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital atresia of duodenum |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital melanosis of sclera |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
4 |
Epitheliogenesis imperfecta lingua bovis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Bifid thumb |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
syndrome de Cayler |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cranio-orbito-ocular dysraphia syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Acquired pulsion diverticulum of esophagus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital atresia of aortic valve (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Complete trisomy 18 syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Marginal insertion of umbilical cord |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital laryngocele |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Ectopic anus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Werner syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital malaria |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital absence of all fingers |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital anomaly of skull |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital absence of prostate |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Taurodontism |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cerebro-costo-mandibular syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital malposition of cardiac apex |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital anomaly of ureter |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Disorder of tryptophan metabolism |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
17p partial trisomy syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Prune belly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Akabane virus disease |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Spondyloepiphyseal dysplasia tarda |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Dysmorphic sialidosis, infantile form |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
Congenital bent nose (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital absence of ulna |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
dégénérescence myxomateuse d'une valve cardiaque |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital human immunodeficiency virus infection |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Infantile lobar overinflation of lung |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Enlarged tongue |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Universal mesentery |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Niemann-Pick disease, type A |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Ocular albinism-lentigines-deafness syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Dysmorphic sialidosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
HNSHA due to glutathione reductase deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Intermittent branched-chain ketonuria |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Linear sebaceous nevus sequence |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital absence of coronary artery |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Homocystinemia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Fetal disproportion due to fetal myelomeningocele |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Meningoencephalocele |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
HNSHA due to glucose phosphate isomerase deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|