| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Intellectual disability Buenos Aires type (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Neurofaciodigitorenal syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Caudal appendage deafness syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
8 |
| Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
8 |
| Weaver Williams syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Intellectual disability, cataract, calcified pinna, myopathy syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| X-linked intellectual disability Hedera type (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| X-linked intellectual disability Nascimento type (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Cortical blindness, intellectual disability, polydactyly syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Osteopenia, intellectual disability, sparse hair syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Brachydactyly and preaxial hallux varus syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Spastic paraplegia with precocious puberty syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Branchial dysplasia, intellectual disability, inguinal hernia syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Epilepsy telangiectasia syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Dysmorphism, short stature, deafness, disorder of sex development syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Marfanoid habitus with autosomal recessive intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Stimmler syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
8 |
| Pseudoprogeria syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
8 |
| Preaxial polydactyly, colobomata, intellectual disability syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Van den Bosch syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Aniridia, renal agenesis, psychomotor retardation syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Thumb stiffness, brachydactyly, intellectual disability syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Trigonocephaly C syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Skeletal dysplasia with epilepsy and short stature syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| McDonough syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Goniodysgenesis with intellectual disability and short stature syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Harrod syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Hypospadias and intellectual disability syndrome Goldblatt type (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Early onset parkinsonism and intellectual disability syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Microcephaly with deafness and intellectual disability syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Alopecia and intellectual disability syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Intellectual disability and short stature with hand contracture and genital anomaly syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Female restricted epilepsy with intellectual disability syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| FRAXE intellectual disability syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| L1 syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Trisomy 10p (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Microphthalmia with ankyloblepharon and intellectual disability syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Wolf Hirschhorn syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
9 |
| Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Spastic paraplegia, glaucoma, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Microcephalus, glomerulonephritis, marfanoid habitus syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Megalocornea with intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| SCARF syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Temtamy preaxial brachydactyly syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Blepharophimosis, intellectual disability syndrome, Verloes type (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Severe intellectual disability and progressive spastic paraplegia |
Has interpretation |
False |
Impaired |
Inferred relationship |
Some |
6 |
| Atypical hypotonia cystinuria syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| SYNGAP1-related intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Severe intellectual disability, progressive spastic diplegia syndrome (disorder) |
Has interpretation |
False |
Impaired |
Inferred relationship |
Some |
5 |
| Intellectual disability, facial dysmorphism syndrome due to SET domain containing 5 haploinsufficiency (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Congenital muscular dystrophy with intellectual disability and severe epilepsy |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Hereditary cryohydrocytosis with reduced stomatin |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Richieri Costa-da Silva syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
8 |
| Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Macrocephaly, intellectual disability, autism syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Congenital muscular dystrophy with intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| X-linked intellectual disability due to GRIA3 mutations |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Muscle eye brain disease with bilateral multicystic leukodystrophy |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
8 |
| Hyperekplexia epilepsy syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| 21q22.11q22.12 microdeletion syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Ankyrin 3 related intellectual disability, sleep disturbance syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| 14q32 deletion syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Mowat-Wilson syndrome due to monosomy 2q22 (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| X-linked complicated corpus callosum dysgenesis (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Contracture with ectodermal dysplasia and orofacial cleft syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
10 |
| X-linked intellectual disability Brooks type (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| X-linked intellectual disability hypotonic face syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Angelman syndrome due to maternal monosomy 15q11q13 (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Microcephaly, corpus callosum and cerebellar vermis hypoplasia, facial dysmorphism, intellectual disability syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Tall stature, intellectual disability, renal anomalies syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| RERE-related neurodevelopmental syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Early-onset epilepsy, intellectual disability, brain anomalies syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |