| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| X-linked intellectual disability, hypotonia, movement disorder syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Congenital contracture of limbs and face, hypotonia, developmental delay syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| X-linked intellectual disability, short stature, overweight syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Baraitser Winter cerebrofrontofacial syndrome (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Menke Hennekam syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| WARS2-related combined oxidative phosphorylation defect |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Megalencephaly, severe kyphoscoliosis, overgrowth syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| GRIN2B-related developmental delay, intellectual disability, autism spectrum disorder |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Infantile multisystem neurologic, endocrine, pancreatic disease (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Spondylometaphyseal dysplasia, corneal dystrophy syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Primary hypomagnesemia, refractory seizures, intellectual disability syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Combined oxidative phosphorylation defect type 39 |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
| Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|