| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Syndromic X-linked intellectual disability due to JARID1C mutation | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| W syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked recessive sensory neuropathy | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Ocular albinism, type I | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Chondrodysplasia punctata, X-linked recessive type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability with seizure and psoriasis syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked cone dysfunction syndrome with myopia | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Hydrocephalus with obesity and hypogonadism syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Brunner syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability with ataxia and apraxia syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Chromosome Xp11.3 microdeletion syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| SCARF syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability with cubitus valgus and dysmorphism syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Microphthalmia with ankyloblepharon and intellectual disability syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked epilepsy with learning disability and behaviour disorder syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Shrimpton type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Pai type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| N syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked spasticity, intellectual disability, epilepsy syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked severe congenital neutropenia | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Lethal ataxia-deafness-optic atrophy | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Juberg Marsidi syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Intellectual disability, developmental delay, contracture syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Alpha thalassaemia X-linked intellectual disability syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked Charcot-Marie-Tooth disease type 4 | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked Charcot-Marie-Tooth disease type 3 | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Abruzzo Erickson syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Spastic paraplegia type 2 | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked Charcot-Marie-Tooth disease type 5 | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked endothelial corneal dystrophy | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked myopathy with excessive autophagy | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked hereditary sensory and autonomic neuropathy with deafness | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Deafness and intellectual disability Martin Probst type syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Pierre Robin sequence faciodigital anomaly syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Bullous dystrophy macular type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked Charcot-Marie-Tooth disease type 2 | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Morse Rawnsley Sargent syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Hoyeraal-Hreidarsson syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Deafness and hypogonadism syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Van Esch type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behaviour syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked spinocerebellar ataxia type 3 | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Aland Islands eye disease | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Cilliers type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked spondyloepimetaphyseal dysplasia | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked parkinsonism with spasticity syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Xq12-q13.3 duplication syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked progressive cerebellar ataxia | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked spinocerebellar ataxia type 4 | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked osteoporosis with fractures | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Xp22.13p22.2 duplication syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Snyder type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Seemanova type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Siderius type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Stevenson type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Stocco Dos Santos type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Stoll type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Schimke type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Miles-Carpenter type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Cantagrel type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Armfield type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Nascimento type | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked retinal dysplasia | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| 3-Methylglutaconic aciduria type 2 | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Corpus callosum agenesis, abnormal genitalia syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Cerebellum agenesis with hydrocephaly | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Albinism with deafness syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Borjeson-Forssman-Lehmann syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Atrophia bulborum hereditaria | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Bulbospinal neuronopathy | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Blue cone monochromatism | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Beta thalassaemia X-linked thrombocytopenia syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Brachytelephalangic chondrodysplasia punctata | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Cutis laxa, x-linked | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Congenital adrenal hypoplasia, X-linked | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| CK syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Contiguous ABCD1 DXS1357E deletion syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Chromosome Xq27.3q28 duplication syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Choroideraemia | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| SSR4-CDG - signal sequence receptor subunit 4 congenital disorder of glycosylation | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Congenital disorder of glycosylation type 1s | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Danon disease | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Deafness-dystonia-optic neuronopathy syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Dent's disease | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome, type 5 | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Distal Xq28 microduplication syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Early-onset X-linked optic atrophy | Is a | False | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Early onset parkinsonism and intellectual disability syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Ferro-cerebro-cutaneous syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Fried syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| FRAXE intellectual disability syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| L1 syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Hyperekplexia epilepsy syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Infantile epileptic dyskinetic encephalopathy | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  |