Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital anomaly of peripheral nerve |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Achondrogenesis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Ectopic splenic tissue |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Imperfect fusion of skull |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Funicular hernia of umbilical cord |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Anomaly of dental arch |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Hyperleucinemia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Median mandibular cyst |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Complete bilateral cleft palate |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital chorioretinal degeneration |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Distal arthrogryposis syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital dilatation of colon |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Xiphopagus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cystathionine beta-synthase deficiency |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Metachromatic leukodystrophy, adult type |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Meromicrosomia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Accessory thymic tissue |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Iniencephaly |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Thoracodelphus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Mutilating keratoderma |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Primary gout |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Accessory eyelid |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Laterality sequence |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Posterior open bite |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Metaphyseal chondrodysplasia, Jansen type |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
G-6-PD class III variant anemia |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
4 |
Thoracopagus parasiticus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Townes syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Infantile cortical hyperostosis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
7p partial monosomy (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital absence of broad ligament |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Potter's facies |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital postural lordosis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital cerebral arteriovenous aneurysm (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital anomaly of sternocleidomastoid muscle |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Benign adult cystinosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Hydromeningocele |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital absence of uvula |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
HNSHA due to gamma glutamyl cysteine synthetase deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Coalition of calcaneus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Hereditary spherocytosis due to spectrin deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Longitudinal deficiency of phalanges of foot |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Uterus parvicollis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital absence of vena cava |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
HSMN IV |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
5 |
Aqueduct of Sylvius anomaly |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Primordial cyst |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Autosomal recessive glutaric aciduria, type 2 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
1 |
X chromosome-linked pyridoxine responsive sideroblastic anemia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital absence of left pulmonary artery |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Syndactyly of fingers with fusion of bones |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Ehlers-Danlos syndrome, hydroxylysine-deficient |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital duodenal obstruction due to malrotation of intestine |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital fissure of sternum |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Isolated cystinuria |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Hyperhydroxyprolinemia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Neonatal iminoglycinuria |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Xeroderma pigmentosum, group C (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Kearns-Sayre syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Chiari's network |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital atresia of ileum |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Dubowitz's syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital absence of rectum (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Bone island |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Maroteaux-Lamy syndrome, intermediate form |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Congenital absence of external auditory canal |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Microcornea |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
5-Oxoprolinase deficiency |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Complete transposition of great vessels |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Ectopic bone tissue, congenital |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital atresia of esophagus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Frog fetus |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Aortic left ventricular tunnel |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Senter syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Chronic granulomatous disease, type IIA |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Uterus incudiformis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital obstruction of small intestine |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Tyrosinase-positive oculocutaneous albinism |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Ocular albinism |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital tracheocele |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital dyserythropoietic anemia, type III |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
5 |
Agyria |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cat eye syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
11p partial trisomy syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Faun tail syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Congenital ectropion |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Syringobulbia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital absence of part of brain |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Anodontia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Robinson nail dystrophy-deafness syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Persistent thyroglossal duct |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Mucopolysaccharidosis, MPS-I-H/S |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Coarctation of pulmonary artery |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital absence of superior vena cava |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cervical auricle |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Dominant dystrophic epidermolysis bullosa with absence of skin |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Coronary ostium stenosis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Anterior crossbite |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|