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{{Navbox
| name = X-linked disorders
| title = [[Sex linkage|X-linked]] disorders
| state = {{{state|autocollapse}}}
| listclass = hlist

| list1 =
{{Navbox|child
| title = [[X-linked recessive inheritance|X-linked recessive]]
| listclass = hlist
| state = {{{state|plain}}}

| group1 = [[Immune disorder|Immune]]
| list1 =
* [[Chronic granulomatous disease|Chronic granulomatous disease (CYBB)]]
* [[Wiskott–Aldrich syndrome]]
* [[X-linked severe combined immunodeficiency]]
* [[X-linked agammaglobulinemia]]
* [[Hyper-IgM syndrome type 1]]
* [[IPEX syndrome|IPEX]]
* [[X-linked lymphoproliferative disease]]
* [[Properdin deficiency]]

| group2 = [[Hematologic disease|Hematologic]]
| list2 =
* [[Haemophilia A]]
* [[Haemophilia B]]
* [[Sideroblastic anemia|X-linked sideroblastic anemia]]

| group3 = [[Endocrine disease|Endocrine]]
| list3 =
* [[Androgen insensitivity syndrome]]/[[Spinal and bulbar muscular atrophy]]
* [[Kallmann syndrome|KAL1 Kallmann syndrome]]
* [[X-linked adrenal hypoplasia congenita]]

| group4 = [[Metabolic disorder|Metabolic]]
| list4 =
* ''[[Congenital disorders of amino acid metabolism|Amino acid]]:'' [[Ornithine transcarbamylase deficiency]]
* [[Oculocerebrorenal syndrome]]

* ''[[Dyslipidemia]]:'' [[Adrenoleukodystrophy]]

* ''[[Carbohydrate metabolism]]:'' [[Glucose-6-phosphate dehydrogenase deficiency]]
* [[Pyruvate dehydrogenase deficiency]]
* [[Danon disease|Danon disease/glycogen storage disease Type IIb]]

* ''[[Lipid storage disorder]]'': [[Fabry disease]]

* ''[[Mucopolysaccharidosis]]:'' [[Hunter syndrome]]

* ''[[Inborn errors of purine–pyrimidine metabolism|Purine–pyrimidine metabolism]]:'' [[Lesch–Nyhan syndrome]]

* ''[[Mineral (nutrient)|Mineral]]:'' [[Menkes disease]]/[[Occipital horn syndrome]]

| group5 = [[Nervous system disease|Nervous system]]
| list5 =
* ''[[X-linked intellectual disability]]:'' [[Coffin–Lowry syndrome]]
* [[MASA syndrome]]
* [[Alpha-thalassemia mental retardation syndrome]]
* [[PHF8]]

* ''Eye disorders:'' [[Color_blindness#Genetic_modes_of_inheritance|Color blindness (red and green, but not blue)]]
* [[Ocular albinism]] ([[Ocular albinism type 1|1]])
* [[Norrie disease]]
* [[Choroideremia]]

* ''Other:'' [[Charcot–Marie–Tooth disease|Charcot–Marie–Tooth disease (CMTX2-3)]]
* [[Pelizaeus–Merzbacher disease]]
* [[X-linked spinal muscular atrophy type 2|SMAX2]]

| group6 = [[Skin condition|Skin]] and related tissue
| list6 =
* [[Dyskeratosis congenita]]
* [[Hypohidrotic ectodermal dysplasia|Hypohidrotic ectodermal dysplasia (EDA)]]
* [[X-linked ichthyosis]]
* [[X-linked endothelial corneal dystrophy]]

| group7 = [[Neuromuscular disease|Neuromuscular]]
| list7 =
* [[Becker muscular dystrophy]]/[[Duchenne muscular dystrophy|Duchenne]]
* [[Centronuclear myopathy|Centronuclear myopathy (MTM1)]]
* [[Conradi–Hünermann syndrome]]
* [[Emery–Dreifuss muscular dystrophy|Emery–Dreifuss muscular dystrophy 1]]

| group8 = [[Urologic disease|Urologic]]
| list8 =
* [[Alport syndrome]]
* [[Dent's disease]]
* [[Nephrogenic diabetes insipidus|X-linked nephrogenic diabetes insipidus]]

| group9 = [[Bone]]/[[tooth]]
| list9 =
* [[Amelogenesis imperfecta|AMELX Amelogenesis imperfecta]]

| group10 = No primary system
| list10 =
* [[Barth syndrome]]
* [[McLeod syndrome]]
* [[Smith–Fineman–Myers syndrome]]
* [[Simpson–Golabi–Behmel syndrome]]
* [[Mohr–Tranebjærg syndrome]]
* [[Nasodigitoacoustic syndrome]]
}}

| list2 =
{{Navbox|child
| title = [[X-linked dominant inheritance|X-linked dominant]]
| listclass = hlist
;
| state = plain

| group1 =
| list1 =
* [[X-linked hypophosphatemia]]
* [[Focal dermal hypoplasia]]
* [[Fragile X syndrome]]
* [[Aicardi syndrome]]
* [[Incontinentia pigmenti]]
* [[Rett syndrome]]
* [[CHILD syndrome]]
* [[Lujan–Fryns syndrome]]
* [[Orofaciodigital syndrome 1]]
* [[Craniofrontonasal dysplasia]]
}}

}}<noinclude> {{noindex-template}}
{{Documentation}}
</noinclude>

Template:X-linked disorders - Revision history

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