| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Amish lethal microcephaly (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Dentin dysplasia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary skin peeling syndrome (disorder) |
Is a |
False |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Xeroderma pigmentosum |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Dysmorphic sialidosis, congenital form |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Dentinogenesis imperfecta |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Curry-Hall syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| 7p22.1 microduplication syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Congenital hereditary endothelial dystrophy (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Chromosome Xp22.3 microdeletion syndrome (disorder) |
Is a |
False |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Beta-D-mannosidosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Choroideremia with deafness and obesity syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Chromosome Xq27.3q28 duplication syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Xq12-q13.3 duplication syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| X-linked intellectual disability hypotonic face syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| 3q29 microdeletion syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| 2p21 microdeletion syndrome without cystinuria (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| 2p21 microdeletion syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Developmental absence of tooth |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Acromesomelic dysplasia Hunter-Thompson type (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Symphalangism Cushing type |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| XK aprosencephaly syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Rieger syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Isomerism of right atrial appendage (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Diaphyseal dysplasia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Ghosal hematodiaphyseal dysplasia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Chondrodysplasia punctata, X-linked dominant type (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Chondrodysplasia punctata, X-linked recessive type |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| N syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Microcephaly, corpus callosum and cerebellar vermis hypoplasia, facial dysmorphism, intellectual disability syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| MARCH syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Tall stature, intellectual disability, renal anomalies syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Deafness-dystonia-optic neuronopathy syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Ocular anomalies, axonal neuropathy, developmental delay syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| RERE-related neurodevelopmental syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Early-onset epilepsy, intellectual disability, brain anomalies syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| TBCK-related intellectual disability syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| SIX homeobox 2-related frontonasal dysplasia (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Microcephaly, congenital cataract, psoriasiform dermatitis syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome |
Is a |
False |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Allan-Herndon-Dudley syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| X-linked agammaglobulinemia with growth hormone deficiency |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Christianson syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| X-linked neurodegenerative syndrome Hamel type (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Combined oxidative phosphorylation defect type 23 |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Severe X-linked myotubular myopathy (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Lethal tight skin contracture syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Mohr syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Orofacial-digital syndrome III |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Orofacial-digital syndrome IV |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Kallman syndrome with heart disease (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Colobomatous macrophthalmia with microcornea syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Familial patent arterial duct |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| CHD3-related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| FLNA-related X-linked myxomatous valvular dysplasia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| GNB5-related intellectual disability, cardiac arrhythmia syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Growth delay, intellectual disability, hepatopathy syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Infantile inflammatory bowel disease with neurological involvement (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Gabriele-de Vries syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Non-specific syndromic intellectual disability |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Familial steroid-resistant nephrotic syndrome with adrenal insufficiency |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Micrognathia, recurrent infections, behavioural abnormalities, mild intellectual disability syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Stromme syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Witteveen Kolk syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Sugarman brachydactyly (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Intellectual disability, epilepsy, extrapyramidal syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| VPS11-related autosomal recessive hypomyelinating leukodystrophy |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Seizures, scoliosis, macrocephaly syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Short stature, brachydactyly, obesity, global developmental delay syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Spastic paraplegia, severe developmental delay, epilepsy syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Intellectual disability, spasticity, ectrodactyly syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Macrocephaly, intellectual disability, left ventricular non compaction syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Basel Vanagaite Smirin Yosef syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
| Melorheostosis with osteopoikilosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|