Freeman–Sheldon syndrome
rare congenital disorder
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Freeman–Sheldon syndrome
Summary
Freeman–Sheldon syndrome is a rare disease[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Freeman–Sheldon syndrome's instance of is recorded as rare disease[3].
- Freeman–Sheldon syndrome's instance of is recorded as genetic disease[4].
- Freeman–Sheldon syndrome's instance of is recorded as class of disease[5].
- Freeman–Sheldon syndrome is a type of distal arthrogryposis[6].
- Freeman–Sheldon syndrome's Commons category is recorded as Freeman–Sheldon syndrome[7].
- Freeman–Sheldon syndrome's NCI Thesaurus ID is recorded as C98931[8].
- Freeman–Sheldon syndrome's health specialty is recorded as medical genetics[9].
- Freeman–Sheldon syndrome's genetic association is recorded as MYH3[10].
Why It Matters
Freeman–Sheldon syndrome has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 3 alternative names across languages and contexts.[11]