| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| CHD3-related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Gabriele-de Vries syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| STAG1-related intellectual disability, facial dysmorphism, gastrooesophageal reflux syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Mucopolysaccharidosis-like plus disease |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Mucopolysaccharidosis-like plus disease |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Micrognathia, recurrent infections, behavioural abnormalities, mild intellectual disability syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Micrognathia, recurrent infections, behavioural abnormalities, mild intellectual disability syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Stromme syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Witteveen Kolk syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Sugarman brachydactyly (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Tubulinopathy-associated dysgyria (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Macrocephaly, intellectual disability, left ventricular non compaction syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Macrocephaly, intellectual disability, left ventricular non compaction syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Basel Vanagaite Smirin Yosef syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Osteogenesis imperfecta, type IV B |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Hallermann Streiff like syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Sanjad Sakati syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Posterior meningocele |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Microform holoprosencephaly |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Autosomal recessive dysgenesis of anterior segment of eye |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Familial cavitary optic disc anomaly (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Intellectual disability, expressive aphasia, facial dysmorphism syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Congenital brachyoesophagus, intrathoracic stomach, vertebral anomalies syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
5 |
| Dieulafoy lesion of small intestine |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Dieulafoy lesion of small intestine |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Congenital fiber-type disproportion myopathy due to ZAK mutation |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Congenital fiber-type disproportion myopathy due to SELENON mutation |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Autosomal dominant congenital fibre-type disproportion myopathy due to SELENON mutation |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Autosomal recessive congenital fiber-type disproportion myopathy due to selenoprotein N mutation (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Dysraphism, cleft lip and palate, limb reduction defect syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
4 |
| Severe oculo-renal-cerebellar syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Eye defects, arachnodactyly, cardiopathy syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Eye defects, arachnodactyly, cardiopathy syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Fryns Smeets Thiry syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Congenital hydrocephalus, low insertion of umbilicus syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Congenital hydrocephalus, low insertion of umbilicus syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Congenital fibre-type disproportion myopathy due to ACTA1 mutation |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Autosomal recessive congenital fibre-type disproportion myopathy due to ACTA1 mutation |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Autosomal dominant congenital fibre-type disproportion myopathy due to ACTA1 mutation |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Congenital fiber-type disproportion myopathy due to TPM3 mutation |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Autosomal recessive congenital fiber-type disproportion myopathy due to TPM3 mutation |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Autosomal dominant congenital fiber-type disproportion myopathy due to TPM3 mutation |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Epibulbar lipodermoid, preauricular appendage, polythelia syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| SATB2-associated syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Congenital anomaly of craniovertebral junction (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Autosomal dominant deafness with onychodystrophy syndrome |
Associated morphology |
False |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
5 |
| Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
4 |
| Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Polymicrogyria due to TUBB2B mutation |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
6 |
| PHIP-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
4 |
| Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Joint contractures, developmental delay, Pierre Robin syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Male pseudohermaphroditism due to congenital adrenal hyperplasia (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Female pseudohermaphroditism due to congenital adrenal hyperplasia |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Pseudohermaphroditism due to congenital adrenal hyperplasia (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
4 |
| X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Severe myopia, generalized joint laxity, short stature syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Diaphragmatic hernia, short bowel, asplenia syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
5 |
| Hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, xerostomia syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Ocular motor apraxia Cogan type (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Milk-induced pulmonary disease in infant |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| QRICH1-related intellectual disability, chondrodysplasia syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Fetal encasement syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Keppen Lubinsky syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Pierpont syndrome (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
3 |
| Congenital anomaly of retina of left eye (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Congenital anomaly of right retina |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Congenital abnormality of left lacrimal drainage system (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Congenital abnormality of right lacrimal drainage system (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Congenital abnormality of bilateral lacrimal drainage systems (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
1 |
| Congenital abnormality of bilateral lacrimal drainage systems (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Coronal hypospadias |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Paraspadias |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |
| Penoscrotal hypospadias (disorder) |
Associated morphology |
True |
Morphologically abnormal structure (morphologic abnormality) |
Inferred relationship |
Some |
2 |