iDrugBank

Achondroplasia

MESHD000130

An autosomal dominant disorder that is the most frequent form of short-limb dwarfism. Affected individuals exhibit short stature caused by rhizomelic shortening of the limbs, characteristic facies with frontal bossing and mid-face hypoplasia, exaggerated lumbar lordosis, limitation of elbow extension, GENU VARUM, and trident hand. (Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim, MIM#100800, April 20, 2001)

Synonyms

  • Achondroplasias
  • Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans
  • SADDAN
  • SADDANs
  • SADDAN Dysplasia
  • Dysplasia, SADDAN
  • Dysplasias, SADDAN
  • SADDAN Dysplasias
  • Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans
  • Skeleton-Skin-Brain Syndrome
  • Skeleton Skin Brain Syndrome
  • Skeleton-Skin-Brain Syndromes
  • Syndrome, Skeleton-Skin-Brain
  • Syndromes, Skeleton-Skin-Brain

Source last updated 2026-05-24T15:28:24.502Z