Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Lysine intolerance |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Gastrothoracopagus dipygus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Autositic twin of asymmetrical conjoined twins (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Autositic twin of asymmetrical conjoined twins (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
Cephalodymus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
Acephaly |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Enamel spur |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Cephalodiprosopus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Congenital complex varus foot deformity |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Acephalobrachius |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital forefoot varus |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Congenital rearfoot varus |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Talipes equinovarus (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
Fetal anencephaly (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Talipes equinocavovarus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
Microcephalic primordial dwarfism of Toriello type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Anencephaly without rachischisis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Glaucoma, ectopia, microspherophakia, stiff joint, short stature syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Glaucoma, ectopia, microspherophakia, stiff joint, short stature syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Polysomia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Polysomia (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
Pericardial and diaphragmatic defect syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
Pericardial and diaphragmatic defect syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Pericardial and diaphragmatic defect syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
Pericardial and diaphragmatic defect syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
Neuroectodermal endocrine syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Neuroectodermal endocrine syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
Neuroectodermal melanolysosomal disease (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Neuroectodermal melanolysosomal disease (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Nephrosis, deafness, urinary tract, digital malformation syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital disorder of glycosylation type 1f (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Monosomy 9q22.3 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Monosomy 9q22.3 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Macrocephaly, obesity, mental disability, ocular abnormality syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
Macrocephaly, obesity, mental disability, ocular abnormality syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
Microtia, eye coloboma, imperforation of nasolacrimal duct syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Microtia, eye coloboma, imperforation of nasolacrimal duct syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
Microtia, eye coloboma, imperforation of nasolacrimal duct syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Microspherophakia with metaphyseal dysplasia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Microspherophakia with metaphyseal dysplasia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
Microspherophakia with metaphyseal dysplasia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Carbohydrate deficient glycoprotein syndrome type 2a (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Embryofetopathy caused by methimazole (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
8q13 microdeletion syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
8q13 microdeletion syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
8q13 microdeletion syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
Ligase 4 syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
Laryngeal abductor paralysis with intellectual disability syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Keratin 14 related epidermolysis bullosa simplex (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
Keratin 14 related epidermolysis bullosa simplex (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Kleefstra syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Keutel syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Keutel syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
Keutel syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
Keutel syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
Palmoplantar keratoderma with clinodactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
Palmoplantar keratoderma with clinodactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Palmoplantar keratoderma with clinodactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
Congenital ichthyosis with hypotrichosis syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Congenital ichthyosis with hypotrichosis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Hypospadias, hypertelorism, coloboma, deafness syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
Hypospadias, hypertelorism, coloboma, deafness syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
Hypospadias, hypertelorism, coloboma, deafness syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
syndrome d'hypoplasie nasale et oculaire-hypogonadisme hypogonadotrope |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
syndrome d'hypoplasie nasale et oculaire-hypogonadisme hypogonadotrope |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
syndrome d'hypoplasie nasale et oculaire-hypogonadisme hypogonadotrope |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
syndrome d'hypoplasie nasale et oculaire-hypogonadisme hypogonadotrope |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
syndrome d'hypoplasie nasale et oculaire-hypogonadisme hypogonadotrope |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
9 |
Acute neuronopathic Gaucher's disease |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Hypoparathyroidism, deafness, renal disease syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
8 |
Hypoparathyroidism, deafness, renal disease syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
9 |
Hypoparathyroidism, deafness, renal disease syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
10 |
Hypoparathyroidism, deafness, renal disease syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
11 |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
Hypertelorism Teebi type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
Hypertelorism Teebi type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Hereditary hyperekplexia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Hepatic glycogen synthase deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Hepatic glycogen synthase deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Muscle and heart glycogen synthase deficiency (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
Muscle and heart glycogen synthase deficiency (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
Muscle and heart glycogen synthase deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
6 |
Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |