X-linked disease

Part of

Sub-types of X-linked disease

• Hemophilia A 180 trials
  5 sub-types

  • Severe hemophilia A 50 trials
  • Moderately severe hemophilia A 4 trials
  • Mild hemophilia A 2 trials
  • Hemophilia A with vascular abnormality 0 trials
  • Symptomatic form of hemophilia A in female carriers 0 trials
• X-linked deafness 0 trials · 32 incl. sub-types
  2 sub-types

  • X-linked nonsyndromic hearing loss 0 trials · 32 incl. sub-types Sub-types →
  • X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome 0 trials
• Adrenoleukodystrophy 19 trials · 20 incl. sub-types
  3 sub-types

  • Adrenomyeloneuropathy 7 trials
  • X-linked cerebral adrenoleukodystrophy 4 trials
  • Isolated adrenal insufficiency 0 trials
• X-linked intellectual disability 1 trial · 15 incl. sub-types
  2 sub-types

  • X-linked syndromic intellectual disability 0 trials · 12 incl. sub-types Sub-types →
  • Non-syndromic X-linked intellectual disability 0 trials · 3 incl. sub-types Sub-types →
• X-linked hypophosphatemic rickets 11 trials · 12 incl. sub-types
  2 sub-types

  • X-linked dominant hypophosphatemic rickets 10 trials
  • Hypophosphatemic rickets, X-linked recessive 0 trials
• X-linked lymphoproliferative syndrome 7 trials · 11 incl. sub-types
  2 sub-types

  • X-linked lymphoproliferative disease due to XIAP deficiency 4 trials
  • X-linked lymphoproliferative disease due to SH2D1A deficiency 2 trials
• Wiskott-Aldrich syndrome 10 trials
• X-linked erythropoietic protoporphyria 10 trials
• X-linked dominant disease 0 trials · 10 incl. sub-types
  1 sub-type

  • X-linked dominant hypophosphatemic rickets 10 trials
• X-linked recessive disease 0 trials · 10 incl. sub-types
  12 sub-types

  • X-linked lymphoproliferative disease due to XIAP deficiency 4 trials
  • X-linked lymphoproliferative disease due to SH2D1A deficiency 2 trials
  • Blue cone monochromacy 2 trials
  • Recessive X-linked ichthyosis 2 trials Sub-types →
  • Brunner syndrome 0 trials
  • IFAP syndrome 1, with or without BRESHECK syndrome 0 trials
  • X-linked complicated spastic paraplegia type 1 0 trials
  • X-linked recessive mitochondrial myopathy 0 trials
  • X-linked recessive ocular albinism 0 trials
  • Holoprosencephaly 13, X-linked 0 trials
  • Hypophosphatemic rickets, X-linked recessive 0 trials
  • Retinitis pigmentosa 6 0 trials
• Choroideremia 6 trials
  2 sub-types

  • Choroideremia hypopituitarism 0 trials
  • Total central choroidal atrophy 0 trials
• X-linked myotubular myopathy 4 trials
  2 sub-types

  • X-linked myotubular myopathy-abnormal genitalia syndrome 0 trials
  • Symptomatic form of X-linked centronuclear myopathy in female carriers 0 trials
• X-linked retinoschisis 4 trials
• X-linked Alport syndrome 3 trials
• Hyper-IgM syndrome type 1 3 trials
• Dyskeratosis congenita, X-linked 0 trials · 3 incl. sub-types
  1 sub-type

  • Hoyeraal-Hreidarsson syndrome 3 trials
• Charcot-Marie-Tooth disease type X 1 trial · 2 incl. sub-types
  6 sub-types

  • Charcot-Marie-Tooth disease X-linked dominant 1 1 trial
  • Charcot-Marie-Tooth disease X-linked dominant 6 0 trials
  • Charcot-Marie-Tooth disease X-linked recessive 2 0 trials
  • Charcot-Marie-Tooth disease X-linked recessive 3 0 trials
  • Charcot-Marie-Tooth disease X-linked recessive 4 0 trials
  • Charcot-Marie-Tooth disease X-linked recessive 5 0 trials
• X-linked cone-rod dystrophy 0 trials · 2 incl. sub-types
  4 sub-types

  • Blue cone monochromacy 2 trials
  • X-linked cone-rod dystrophy 1 0 trials
  • X-linked cone-rod dystrophy 2 0 trials
  • X-linked cone-rod dystrophy 3 0 trials
• X-linked Emery-Dreifuss muscular dystrophy 1 trial
  3 sub-types

  • Emery-Dreifuss muscular dystrophy 1, X-linked 0 trials
  • Emery-Dreifuss muscular dystrophy 6, X-linked 0 trials
  • X-linked myopathy with postural muscle atrophy 0 trials
• X-linked chondrodysplasia punctata 1 trial
  2 sub-types

  • X-linked chondrodysplasia punctata 2 1 trial
  • X-linked chondrodysplasia punctata 1 0 trials
• X-linked hydrocephalus with stenosis of the aqueduct of Sylvius 1 trial
• Diabetes insipidus, nephrogenic, X-linked 1 trial
• Spondyloepiphyseal dysplasia tarda, X-linked 1 trial
• Aarskog-Scott syndrome, X-linked 0 trials
• Aland island eye disease 0 trials
• Dyggve-Melchior-Clausen syndrome, X-linked 0 trials
• X-linked Ehlers-Danlos syndrome 0 trials
• X-linked Opitz G/BBB syndrome 0 trials
• X-linked acrogigantism due to Xq26 microduplication 0 trials
• X-linked adrenal hypoplasia congenita 0 trials
  1 sub-type

  • Adrenal hypoplasia, cytomegalic type 0 trials
• X-linked central congenital hypothyroidism with late-onset testicular enlargement 0 trials
• X-linked cerebellar ataxia 0 trials
  9 sub-types

  • X-linked intellectual disability-ataxia-apraxia syndrome 0 trials
  • X-linked non progressive cerebellar ataxia 0 trials
  • X-linked progressive cerebellar ataxia 0 trials
  • X-linked sideroblastic anemia with ataxia 0 trials
  • X-linked spinocerebellar ataxia type 3 0 trials
  • X-linked spinocerebellar ataxia type 4 0 trials
  • Ataxia - deafness - intellectual disability syndrome 0 trials
  • Fragile X-associated tremor/ataxia syndrome 0 trials
  • Spinocerebellar ataxia, X-linked 2 0 trials
• X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome 0 trials
• X-linked complex neurodevelopmental disorder 0 trials
  2 sub-types

  • Developmental and epileptic encephalopathy, 8 0 trials
  • Developmental and epileptic encephalopathy, 9 0 trials
• X-linked congenital hemolytic anemia 0 trials
• X-linked congenital stationary night blindness 0 trials
  2 sub-types

  • Congenital stationary night blindness 1A 0 trials
  • Congenital stationary night blindness 2A 0 trials
• X-linked distal spinal muscular atrophy type 3 0 trials
• X-linked hypohidrotic ectodermal dysplasia 0 trials
• X-linked immunoneurologic disorder 0 trials
• X-linked lethal multiple pterygium syndrome 0 trials
• X-linked lissencephaly with abnormal genitalia 0 trials
• X-linked mandibulofacial dysostosis 0 trials
• X-linked severe congenital neutropenia 0 trials
• X-linked sideroblastic anemia 1 0 trials
• Cone dystrophy, X-linked, with tapetal-like sheen 0 trials
• Epidermodysplasia verruciformis, X-linked 0 trials
• Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders 0 trials
• Exudative vitreoretinopathy 2, X-linked 0 trials
• Leukemia, acute, X-linked 0 trials
• Macular dystrophy, X-linked 0 trials