| ADR Ontology |
| ADR Term |
Chondrodystrophy |
| ADR ID |
BADD_A00912 |
| ADR Hierarchy |
|
| Description |
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) [MeSH] |
| MedDRA Code |
10008723 |
| MeSH ID |
D000130
|
|
ADR Severity Grade (FAERS)
|
|
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ADR Severity Grade (CTCAE)
|
Not Available
|
| Synonym |
| Achondroplasia | Achondroplastic dwarf | Chondrodystrophy | Congenital dwarfism | Achondrogenesis | Achondroplasias | Achondroplasia, Severe, 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 | Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans | SADDAN | SADDANs | SADDAN Dysplasia | Dysplasia, SADDAN | Dysplasias, SADDAN | SADDAN Dysplasias |
|
|
| ADR Related Proteins |
| Protein Name |
UniProt AC |
TTD Target ID |
| Not Available | Not Available | Not Available |
|
| Drugs Leading to the ADR |
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