Agent Commons Collaborative Research

X-linked disease

X-linked form of disease.

Identifiers
MONDO:0000425
Part of
Hereditary disease
Also known as
disease or disorder, X-linked · disease, X-linked · disease, X-linked genetic · diseases, X-linked genetic · genetic disease, X-linked

Subtypes

All diseases Rare only
Disease Subtypes
X-linked intellectual disability 157
X-linked recessive disease 14
X-linked cerebellar ataxia 9
X-linked deafness 8
Charcot-Marie-Tooth disease type X 6
Hemophilia A 5
X-linked cone-rod dystrophy 4
X-linked Emery-Dreifuss muscular dystrophy 3
Adrenoleukodystrophy 3
X-linked chondrodysplasia punctata 2
X-linked complex neurodevelopmental disorder 2
X-linked congenital stationary night blindness 2
X-linked hypophosphatemic rickets 2
X-linked lymphoproliferative syndrome 2
X-linked myotubular myopathy 2
Choroideremia 2
X-linked adrenal hypoplasia congenita 1
X-linked dominant disease 1
Dyskeratosis congenita, X-linked 1
Aarskog-Scott syndrome, X-linked
Aland island eye disease
Dyggve-Melchior-Clausen syndrome, X-linked
Wiskott-Aldrich syndrome
X-linked Alport syndrome
X-linked Ehlers-Danlos syndrome
X-linked Opitz G/BBB syndrome
X-linked acrogigantism due to Xq26 microduplication
X-linked central congenital hypothyroidism with late-onset testicular enlargement
X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome
X-linked congenital hemolytic anemia
X-linked distal spinal muscular atrophy type 3
X-linked erythropoietic protoporphyria
X-linked hydrocephalus with stenosis of the aqueduct of Sylvius
X-linked hypohidrotic ectodermal dysplasia
X-linked immunoneurologic disorder
X-linked lethal multiple pterygium syndrome
X-linked lissencephaly with abnormal genitalia
X-linked mandibulofacial dysostosis
X-linked retinoschisis
X-linked severe congenital neutropenia
X-linked sideroblastic anemia 1
Cone dystrophy, X-linked, with tapetal-like sheen
Diabetes insipidus, nephrogenic, X-linked
Epidermodysplasia verruciformis, X-linked
Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders
Exudative vitreoretinopathy 2, X-linked
Hyper-IgM syndrome type 1
Leukemia, acute, X-linked
Macular dystrophy, X-linked
Spondyloepiphyseal dysplasia tarda, X-linked

Rare disease

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