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 |
|
Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
SET domain containing 2, histone lysine methyltransferase-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Clark Baraitser syndrome (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Congenital pontocerebellar hypoplasia type 11 (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
SMARCA2-related blepharophimosis, intellectual disability syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Blepharophimosis, intellectual disability syndrome/genitopatellar overlap syndrome (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Dysequilibrium syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
AMeD syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
CIMDAG syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Chromodomain helicase DNA binding protein 4-related neurodevelopmental disorder (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Cleft palate, congenital heart defect, intellectual disability syndrome (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
CPE-related Prader-Willi-like syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Intellectual disability, cupped ears syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Lysine demethylase 3B-related intellectual disability, facial dysmorphism, short stature syndrome (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Primary hypomagnesaemia, generalised seizures, intellectual disability, obesity syndrome |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Epidermal growth factor-related primary hypomagnesemia with intellectual disability (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome (disorder) |
Is a |
True |
Intellectual disability |
Inferred relationship |
Some |
|