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Achondroplasia

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)

Subtype terms (1)

More specific conditions that are subtypes of Achondroplasia in the MeSH hierarchy.

Drugs by status

Approved for this indication (1)

Phase 4 trials (1)

Phase 1 trials (1)

Organizations

Organization Involved with Phase 3 Indications (1)