| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Pallister W syndrome (disorder) | 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 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability with seizure and psoriasis syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked cone dysfunction syndrome with myopia (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Hydrocephalus with obesity and hypogonadism syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Deficiency of monoamine oxidase A (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability with ataxia and apraxia syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Chromosome Xp11.3 microdeletion syndrome (disorder) | 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 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Microphthalmia with ankyloblepharon and intellectual disability syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked epilepsy with learning disability and behavior disorder syndrome (disorder) | 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 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| N syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked spasticity, intellectual disability, epilepsy syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked severe congenital neutropenia (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Arts syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Juberg Marsidi syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Intellectual disability, developmental delay, contracture syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Alpha thalassemia X-linked intellectual disability syndrome (disorder) | 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 |  | 
| X-linked spastic paraplegia type 2 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked Charcot-Marie-Tooth disease type 5 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked endothelial dystrophy of cornea (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked myopathy with excessive autophagy (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked hereditary sensory and autonomic neuropathy with deafness (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Deafness and intellectual disability Martin Probst type syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Pierre Robin sequence faciodigital anomaly syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Bullous dystrophy macular type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked Charcot-Marie-Tooth disease type 2 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Hoyeraal-Hreidarsson syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Deafness and hypogonadism syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Van Esch type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked spinocerebellar ataxia type 3 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Aland Islands eye disease (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Cilliers type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked spondyloepimetaphyseal dysplasia (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked parkinsonism with spasticity syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Xq12-q13.3 duplication syndrome (disorder) | 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 (disorder) | 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 |  | 
| Snyder-Robinson syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Seemanova type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Siderius type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Stevenson type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Stocco Dos Santos type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Stoll type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Schimke type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Miles Carpenter type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Cantagrel type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Armfield type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked intellectual disability Nascimento type (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked retinal dysplasia (disorder) | 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 |  | 
| Agenesis of corpus callosum and abnormal genitalia syndrome | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder) | 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 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder) | 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 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Beta thalassemia X-linked thrombocytopenia syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Brachytelephalangic chondrodysplasia punctata (disorder) | 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 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Chromosome Xq27.3q28 duplication syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Choroideremia | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Congenital disorder of glycosylation type 1y | 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 | False | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Deafness-dystonia-optic neuronopathy syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Dent's disease (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| X-linked Ehlers-Danlos syndrome | 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 (disorder) | Is a | False | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Early onset parkinsonism and intellectual disability syndrome (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) | 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 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| FRAXE intellectual disability syndrome (disorder) | 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 (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  | 
| Infantile epileptic dyskinetic encephalopathy (disorder) | Is a | True | X-linked recessive hereditary disease | Inferred relationship | Some |  |