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Category:Genetic disorders by system

From WikiMD's medical encyclopedia

Subcategories

This category has the following 7 subcategories, out of 7 total.

A

  • ► Albinism‎ (5 P)

E

  • ► Ehlers–Danlos syndrome‎ (5 P)

G

  • ► Genodermatoses‎ (289 P)

H

  • ► Haemophilia‎ (8 P)
  • ► Huntington's disease‎ (8 P)

M

  • ► Muscular dystrophy‎ (51 P)

N

  • ► Neurogenetic disorders‎ (21 P)

Pages in category "Genetic disorders by system"

The following 15 pages are in this category, out of 15 total.

A

  • Amelogenesis imperfecta
  • Anauxetic dysplasia
  • Anemia sideroblastic and spinocerebellar ataxia
  • Asperger syndrome

C

  • Char
  • Choroideremia
  • Cleft lip palate incisor and finger anomalies
  • Color blindness
  • Congenital generalized lipodystrophy
  • Congenital generalized lipodystrophy type 1
  • Tubular aggregate myopathy

J

  • Spondylothoracic dysostosis

O

  • Osteopetrosis

S

  • Sideroblastic anemia

V

  • Vitiligo
Retrieved from "https://wikimd.org/w/index.php?title=Category:Genetic_disorders_by_system&oldid=6183158"
Categories:
  • Genetic diseases and disorders
  • Diseases and disorders by system
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  • This page was last edited on 27 January 2025, at 03:48.
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