| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Congenital absence of bladder and urethra (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Partial anomalous pulmonary venous connection of part of right lung (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Hadziselimovic syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Hadziselimovic syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Hadziselimovic syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Bipartite ossification of supraoccipital bone |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Prune belly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Atrioventricular septal defect with restrictive ventricular component (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Brachymorphism with onychodysplasia and dysphalangism syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Brachymorphism with onychodysplasia and dysphalangism syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Common arterial trunk with obstruction of aortic arch (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Lissencephaly with cerebellar hypoplasia type F |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Achondrogenesis |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Worth disease |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Aortico-left ventricular tunnel with intracardiac aneurysm of septal portion (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Anodontia of primary dentition |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Polyostotic fibrous dysplasia of bone |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Congenital pontocerebellar hypoplasia type 1 (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Hypospadias, penoscrotal |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Partial anomalous pulmonary venous connection of part of left lung (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| X-linked retinal dysplasia (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Idiopathic multicentric osteolysis |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Atresia and stenosis of aorta |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Ullrich congenital muscular dystrophy |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Ectodermal dysplasia with hair-tooth-nail defects |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Nievergelt's syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Cardiocranial syndrome Pfeiffer type (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Bilateral muscular infundibula |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Aortico-left ventricular tunnel of simple type (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Cervical hemivertebra |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Ectodermal dysplasia and sensorineural deafness syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Ectodermal dysplasia and sensorineural deafness syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Frontonasal dysplasia sequence |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Heide syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Heide syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Right superior vena cava connecting to coronary sinus (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Right superior vena cava connecting to coronary sinus (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Arteriovenous malformation of face (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Carpenter-Waziris syndrom |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
1 |
| Congenital partial portal-systemic shunt |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Melorheostosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Melorheostosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Cutaneous lesion resulting from spinal dysraphism (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
1 |
| Hall Riggs syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Hall Riggs syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Hall Riggs syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Venous remnant |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Incomplete ossification of zygomatic bone |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Microtia |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Congenital degeneration of nervous system |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Osteogenesis imperfecta, dominant perinatal lethal |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Wolcott-Rallison dysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Ectodermal dysplasia with sweating defect |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Congenital urethrovaginal fistula (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Congenital transverse mandibular hypoplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
4 |
| Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
5 |
| Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Trichothiodystrophy (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Trichothiodystrophy (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Sacral spina bifida without hydrocephalus - open (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Congenital eventration of right crus of diaphragm |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| kongenital anomali av foster |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
1 |
| Mannosidosis, type II (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Ameloonychohypohidrotic syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Straddling tricuspid valve |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Agenesis of left kidney co-occurrent with congenital dysplasia of right kidney (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Maxillary dysostosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Cicatricial junctional epidermolysis bullosa |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Café-au-lait macules with temporal dysrhythmia (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Phocomelia |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Naxos disease |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Metaphyseal chondrodysplasia, Sedaghatian type (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Double inlet ventricle |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Desbuquois syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Isolation of branch of aortic arch |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Dermatoosteolysis Kirghizian type (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Dermatoosteolysis Kirghizian type (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Salamon's syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Pelviscapular dysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Right ventricular outflow tract obstruction due to septal hypertrophy (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
1 |
| Partial anomalous pulmonary venous connection with anomalous veins connecting first to pulmonary venous confluence (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| syndrom med mikrocefali, intellektuell funktionsnedsättning samt falangeal och neurologisk anomali |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
1 |
| syndrom med mikrocefali, intellektuell funktionsnedsättning samt falangeal och neurologisk anomali |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
2 |
| Genochondromatosis type 2 (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Prune belly syndrome with pulmonic stenosis, mental retardation and deafness |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Microcornea with glaucoma and absent frontal sinus syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| dysplasigrupp med korta revben, med eller utan polydaktyli |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
1 |
| Brachytelephalangy, facial dysmorphism, Kallmann syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Gnathodiaphyseal dysplasia syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |