| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Choroideraemia with deafness and obesity syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Chudley Lowry Hoar syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Deafness and intellectual disability Martin Probst type syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Holmes Gang syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Hydrocephalus with obesity and hypogonadism syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Juberg Marsidi syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Microphthalmia with linear skin defect syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| BRESEK syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Intellectual disability, balding, patella luxation, acromicria syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Oto-palato-digital syndrome, type II |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Oto-palato-digital syndrome, type I |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Ocular albinism with late-onset sensorineural deafness |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Albinism with deafness syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Intellectual disability, developmental delay, contracture syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Skeletal dysplasia with intellectual disability syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Early-onset X-linked optic atrophy |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Orofaciodigital syndrome type 8 |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Severe X-linked mitochondrial encephalomyopathy |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Severe X-linked intellectual disability Gustavson type |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked congenital dyserythropoietic anaemia with thrombocytopenia |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| N syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Terminal osseous dysplasia and pigmentary defect syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Syndactyly, telecanthus, anogenital and renal malformation syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Spastic paraplegia type 2 |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Simpson Golabi Behmel syndrome type 2 |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Nephrogenic syndrome of inappropriate antidiuresis |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Phosphoribosylpyrophosphate synthetase superactivity |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Pierre Robin sequence faciodigital anomaly syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Renier Gabreels Jasper syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Keratosis follicularis, dwarfism, cerebral atrophy syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| McLeod neuroacanthocytosis syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Lisch epithelial corneal dystrophy |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Laryngeal abductor paralysis with intellectual disability syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked spasticity, intellectual disability, epilepsy syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Aland Islands eye disease |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Hypohidrotic X-linked ectodermal dysplasia |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked muscular dystrophy not predominantly limb girdle |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Bullous dystrophy macular type |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| TARP syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability Brooks type |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked hereditary spastic paraplegia |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability Hedera type |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability Nascimento type |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Xp22.3 microdeletion syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Beta-propeller protein-associated neurodegeneration |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked hyper-IgM syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Congenital disorder of glycosylation type 1s |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Choroideraemia |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Mononen Karnes Senac syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| SSR4-CDG - signal sequence receptor subunit 4 congenital disorder of glycosylation |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Isolated congenital megalocornea |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| SCARF syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| 2-methyl-3-hydroxybutyric aciduria |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Incontinentia pigmenti syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Ocular albinism, type II |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Oculo-palato-digital syndrome |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Adrenomyodystrophy |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked hereditary motor and sensory neuropathy |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked lethal multiple pterygium syndrome |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Intellectual disability, alacrima, achalasia syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Fragile X associated tremor ataxia syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Corpus callosum agenesis, abnormal genitalia syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Oro-facial digital syndrome type 1 |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Xq12-q13.3 duplication syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked agammaglobulinaemia with growth hormone deficiency |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked muscular dystrophy with limb girdle distribution |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X chromosome-linked sideroblastic anaemia |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked non progressive cerebellar ataxia |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked cleft palate and ankyloglossia |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked distal spinal muscular atrophy type 3 |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Otopalatodigital syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked spondyloepimetaphyseal dysplasia |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked cerebral, cerebellar, coloboma syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked parkinsonism with spasticity syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Spinal muscular atrophy with respiratory distress type 2 |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Infantile epileptic dyskinetic encephalopathy |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Absent radius, anogenital anomalies syndrome |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Severe neonatal onset encephalopathy with microcephaly |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Torticollis, keloids, cryptorchidism, renal dysplasia syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|