| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Kagami Ogata syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Alopecia, progressive neurological defect, endocrinopathy syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Hepatic fibrosis, renal cyst, intellectual disability syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, short stature, hypertelorism syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Polymicrogyria with optic nerve hypoplasia | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Pseudoleprechaunism syndrome Patterson type | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Jawad syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Developmental and speech delay due to SRY-box 5 deficiency | Is a | False | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Autism spectrum disorder due to AUTS2 activator of transcription and developmental regulator deficiency | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| 15q overgrowth syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| RAB18, member RAS oncogene family deficiency | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| White Sutton syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Cyclin-dependent kinase-like 5 deficiency | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| X-linked intellectual disability, craniofacioskeletal syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Spondyloepimetaphyseal dysplasia Genevieve type | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Zechi Ceide syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| CK syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Xylosyltransferase 1 congenital disorder of glycosylation | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, facial dysmorphism, hand anomalies syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Severe feeding difficulties, failure to thrive, microcephaly due to ASXL transcriptional regulator 3 deficiency syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Roifman syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability with strabismus syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| 9q31.1q31.3 microdeletion syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Short ulna, dysmorphism, hypotonia, intellectual disability syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| 13q12.3 microdeletion syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| 14q24.1q24.3 microdeletion syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Spondylocostal dysostosis, hypospadias, intellectual disability syndrome | Is a | False | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Distal Xq28 microduplication syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Rare non-syndromic intellectual disability | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, hypotonia, brachycephaly, pyloric stenosis, cryptorchidism syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Pitt Hopkins-like syndrome | Is a | False | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Ataxia, photosensitivity, short stature syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Deafness with onychodystrophy syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Piebald trait with neurologic defects syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, severe speech delay, mild dysmorphism syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Temtamy preaxial brachydactyly syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Blepharophimosis, intellectual disability syndrome, Verloes type | Is a | False | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Atypical hypotonia cystinuria syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Synaptic Ras GTPase activating protein 1- related intellectual disability | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Hereditary cryohydrocytosis with reduced stomatin | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Congenital muscular dystrophy with intellectual disability and severe epilepsy | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, facial dysmorphism syndrome due to SET domain containing 5 haploinsufficiency | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Richieri Costa-da Silva syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion | Is a | False | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Macrocephaly, intellectual disability, autism syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Congenital muscular dystrophy with intellectual disability | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| X-linked intellectual disability due to glutamate ionotropic receptor AMPA type subunit 3 mutations | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion | Is a | False | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Muscle eye brain disease with bilateral multicystic leukodystrophy | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Hyperekplexia epilepsy syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| 21q22.11q22.12 microdeletion syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Ankyrin 3 related intellectual disability, sleep disturbance syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, hyperkinetic movement, truncal ataxia syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Fatal X-linked ataxia with deafness and loss of vision | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Cross syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Hennekam lymphangiectasia-lymphedema syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Gillespie syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Seckel syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Fragile X syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Angelman syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Lowe syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Alopecia, epilepsy, intellectual disability syndrome Moynahan type | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Blepharophimosis, intellectual disability syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Diabetes, hypogonadism, deafness, intellectual disability syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Myhre syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| 14q32 deletion syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| X-linked intellectual disability hypotonic face syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Tetrasomy 12p syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| N syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  | 
| Microcephaly, corpus callosum and cerebellar vermis hypoplasia, facial dysmorphism, intellectual disability syndrome | Is a | True | Intellectual disability | Inferred relationship | Existential restriction modifier |  |