| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Ogden syndrome |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Solute carrier family 35 member A2 congenital disorder of glycosylation |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked central congenital hypothyroidism with late-onset testicular enlargement |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability, craniofacioskeletal syndrome |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Spondyloepimetaphyseal dysplasia Bieganski type |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Spondylometaphyseal dysplasia Golden type |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| CK syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Contiguous ABCD1 DXS1357E deletion syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Distal Xq28 microduplication syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked myopathy with postural muscle atrophy |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Multiple congenital anomalies, hypotonia, seizures syndrome type 2 |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Familial infantile gigantism |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked acrogigantism |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Ferro-cerebro-cutaneous syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Brachytelephalangic chondrodysplasia punctata |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked acrogigantism |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Lesch-Nyhan syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Bulbospinal neuronopathy |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked osteoporosis with fractures |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Xp22.13p22.2 duplication syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked dyserythropoietic anaemia with abnormal platelets and neutropenia |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Male emopamil-binding protein disorder with neurological defect |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked calvarial hyperostosis |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Atypical Rett syndrome |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Cutis laxa, x-linked |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability due to GRIA3 mutations |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Otopalatodigital syndrome spectrum disorder |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked scapuloperoneal muscular dystrophy |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Hyperekplexia epilepsy syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked dominant chondrodysplasia punctata of Happle |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked acrogigantism |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Partial androgen insensitivity syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Focal dermal hypoplasia |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Ehlers-Danlos syndrome, type 5 |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Pelizaeus-Merzbacher disease |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Fragile X syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Lowe syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Aicardi's syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Blue cone monochromatism |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked progressive cerebellar ataxia |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Familial x-linked hypophosphataemic vitamin D refractory rickets |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked asexual dwarfism |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked hypodontia |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked oligodontia |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked congenital generalised hypertrichosis |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability hypotonic face syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked complex hereditary spastic paraplegia |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked pure hereditary spastic paraplegia |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked Emery-Dreifuss muscular dystrophy |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked distal hereditary motor neuropathy |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked thrombocytopaenia with normal platelets |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked recessive hereditary disease |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked dominant hereditary disease |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked sensorineural hearing loss |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked excess of thyroxine-binding globulin |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked reduction of thyroxine-binding globulin |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked absence of thyroxine-binding globulin |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked retinitis pigmentosa |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked variant form of thyroxine-binding globulin |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Panhypopituitarism - X-linked |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Hypoparathyroidism - X-linked |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Xq25 microduplication syndrome |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked optic atrophy |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Atrophia bulborum hereditaria |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Fabry's disease |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Borjeson-Forssman-Lehmann syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Hereditary factor VIII deficiency disease |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Placental sulfatase deficiency |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Hereditary factor IX deficiency disease |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Menkes kinky-hair syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Glycogen storage disease, type VI |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Hereditary nephrogenic diabetes insipidus |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Glucose-6-phosphate dehydrogenase deficiency anaemia |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked agammaglobulinaemia |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Mucopolysaccharidosis, MPS-II |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked hydrocephalus syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked ichthyosis with steryl-sulfatase deficiency |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Congenital adrenal hypoplasia, X-linked |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked lymphoproliferative syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Ocular albinism, type I |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Danon disease |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability with marfanoid habitus |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Simpson-Golabi-Behmel syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Lenz microphthalmia syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Dent's disease |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Nance-Horan syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked periventricular heterotopia |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked dystonia parkinsonism |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked creatine deficiency |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Blepharophimosis-intellectual disability syndrome, Maat-Kievit-Brunner type |
Is a |
True |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Oculofaciocardiodental syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Renpenning syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Allan-Herndon-Dudley syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Christianson syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability-psychosis-macroorchidism syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Partington syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| X-linked intellectual disability Snyder type |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|
| Deafness-dystonia-optic neuronopathy syndrome |
Is a |
False |
X-linked hereditary disease |
Inferred relationship |
Some |
|