Template:X-linked disorders: Difference between revisions

Sex linkage: X-linked disorders

X-linked recessive
Immune	Chronic granulomatous disease (CYBB) · Wiskott-Aldrich syndrome · X-linked severe combined immunodeficiency · X-linked agammaglobulinemia · Hyper-IgM syndrome type 1 · IPEX · X-linked lymphoproliferative disease · Properdin deficiency
Hematologic	Haemophilia A · Haemophilia B · X-linked sideroblastic anemia
Endocrine	Androgen insensitivity syndrome/Kennedy disease · KAL1 Kallmann syndrome · X-linked adrenal hypoplasia congenita
Metabolic	amino acid: Ornithine transcarbamylase deficiency · Oculocerebrorenal syndrome dyslipidemia: Adrenoleukodystrophy carbohydrate metabolism: Glucose-6-phosphate dehydrogenase deficiency · Pyruvate dehydrogenase deficiency · Danon disease/glycogen storage disease Type IIb lipid storage disorder: Fabry's disease mucopolysaccharidosis: Hunter syndrome purine-pyrimidine metabolism: Lesch-Nyhan syndrome mineral: Menkes disease/Occipital horn syndrome
Nervous system	X-Linked mental retardation: Coffin-Lowry syndrome · MASA syndrome · X-linked alpha thalassemia mental retardation syndrome · Siderius X-linked mental retardation syndrome eye disorders: Color blindness (red and green, but not blue) · Ocular albinism (1) · Norrie disease · Choroideremia other: Charcot-Marie-Tooth disease (CMTX2-3) · Pelizaeus-Merzbacher disease · SMAX2
Skin and related tissue	Dyskeratosis congenita · Hypohidrotic ectodermal dysplasia (EDA) · X-linked ichthyosis · X-linked endothelial corneal dystrophy
Neuromuscular	Becker's muscular dystrophy/Duchenne · Centronuclear myopathy (MTM1) · Conradi-Hünermann syndrome · Emery-Dreifuss muscular dystrophy 1
Urologic	Alport syndrome · Dent's disease · X-linked nephrogenic diabetes insipidus
Bone/tooth	AMELX Amelogenesis imperfecta
No primary system	Barth syndrome · McLeod syndrome · Smith-Fineman-Myers syndrome · Simpson-Golabi-Behmel syndrome

X-linked dominant
X-linked hypophosphatemia · Focal dermal hypoplasia · Fragile X syndrome · Aicardi syndrome · Incontinentia pigmenti · Rett syndrome · CHILD syndrome · Lujan-Fryns syndrome

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 | group9style = background:#BBEEBB;
-| group9 = [{Bone]]/[[tooth]]
+| group9 = [[Bone]]/[[tooth]]
 |  list9 = [[Amelogenesis imperfecta|AMELX Amelogenesis imperfecta]]

Revision as of 20:17, 28 December 2010