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Category:Genetic Disorders

From WikiMSK

WikiMSK > Regions > Widespread > Genetic Disorders

Subcategories

This category has the following 4 subcategories, out of 4 total.

G

  • Glycogen Storage Diseases (4 P)

H

  • Heritable Connective Tissue Disorders (8 P)

L

  • Lysosomal Storage Diseases (2 P)

M

  • Mitochondrial Diseases (2 P)

Pages in category "Genetic Disorders"

The following 22 pages are in this category, out of 22 total.

B

  • Brachydactyly

C

  • Channelopathies and Chronic Pain
  • Charcot Marie Tooth Disease
  • Coarse Facies
  • Collagen VI-Related Dystrophies

D

  • Dolichocephaly

E

  • Erythromelalgia

F

  • Facial Dysmorphology
  • Facioscapulohumeral Dystrophy
  • Familial Episodic Pain Syndrome

G

  • Genetic Testing

H

  • Hereditary Neuropathy with liability to Pressure Palsies
  • Hypertelorism

M

  • Micrognathia
  • Midface Hypoplasia
  • Myotonia
  • Myotonia Congenita
  • Myotonic Dystrophy

P

  • Paroxysmal Extreme Pain Disorder

R

  • Rare Diseases

S

  • Sodium Channelopathies

T

  • Triangular Facies
Retrieved from "https://wikimsk.org/w/index.php?title=Category:Genetic_Disorders&oldid=20479"
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  • This page was last edited 18:34, 12 March 2023 by Jeremy Steinberg.
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