Cousin syndrome
genetic disorder
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Cousin syndrome
Summary
Cousin syndrome is a genetic disease[1]. It draws 105 Wikipedia views per month (genetic_disease category, ranking #14 of 16).[2]
Key Facts
- Cousin syndrome's instance of is recorded as genetic disease[3].
- Cousin syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Cousin syndrome's instance of is recorded as rare disease[5].
- Cousin syndrome's instance of is recorded as class of disease[6].
- Cousin syndrome is a type of syndrome with limb reduction defects[7].
- Cousin syndrome is a type of dysostosis of genetic origin with limb anomaly as a major feature[8].
- Cousin syndrome's genetic association is recorded as TBX15[9].
- Cousin syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_93333[10].
Why It Matters
Cousin syndrome draws 105 Wikipedia views per month (genetic_disease category, ranking #14 of 16).[2] It is known by 6 alternative names across languages and contexts.[11]