Category:X-linked recessive disorders: Difference between revisions

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For more information, see X-linked recessive inheritance.

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X-linked_recessive_disorders

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choroideremia

Subcategories

This category has only the following subcategory.

C

• Color blindness (2 P)

Pages in category "X-linked recessive disorders"

The following 37 pages are in this category, out of 37 total.

A

• Acquired hemophilia A
• Aldred syndrome

B

• Barth syndrome
• Becker muscular dystrophy

C

• Cardiomyopathy, X linked, fatal infantile
• Chondrodysplasia punctata 1, X-linked recessive
• Chudley–Lowry–Hoar syndrome
• Color blindness

D

• Duchenne muscular dystrophy
• Dystrophinopathy

G

• Glycerol kinase deficiency

I

• Intellectual disability-developmental delay-contractures syndrome

K

• Spinal and bulbar muscular atrophy

L

• L1 syndrome
• Lujan–Fryns syndrome

M

• MASA syndrome
• McLeod neuroacanthocytosis syndrome
• Menkes disease

N

• Norrie
• Norrie disease

O

• Oculocerebrorenal syndrome

P

• Patterson–Lowry syndrome
• Pterygium syndrome X linked

S

• Snyder–Robinson syndrome

T

• Tranebjaerg–Svejgaard syndrome

W

• Wilson–Turner syndrome
• Wiskott–Aldrich syndrome

X

• X-linked agammaglobulinemia
• X-linked complicated corpus callosum dysgenesis
• X-linked creatine deficiency
• X-linked dystonia-parkinsonism/Lubag
• X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
• X-linked intellectual disability
• X-linked intellectual disability, Siderius type
• X-linked recessive chondrodysplasia punctata
• X-linked recessive disorders
• X-linked severe combined immunodeficiency

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Category:

• Genetic disorders by inheritance