sirenomelia
disease
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sirenomelia
Summary
sirenomelia is a congenital disorder[1]. sirenomelia has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- sirenomelia's instance of is recorded as congenital disorder[3].
- sirenomelia's instance of is recorded as rare disease[4].
- sirenomelia's instance of is recorded as developmental defect during embryogenesis[5].
- sirenomelia's instance of is recorded as class of disease[6].
- sirenomelia is a type of ectromelia[7].
- sirenomelia is a type of familial caudal dysgenesis[8].
- sirenomelia's Commons category is recorded as Sirenomelia[9].
- sirenomelia's NCI Thesaurus ID is recorded as C118455[10].
- sirenomelia's health specialty is recorded as medical genetics[11].
- sirenomelia's genetic association is recorded as VANGL1[12].
- sirenomelia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3169[13].
Why It Matters
sirenomelia has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[2] sirenomelia is known by 18 alternative names across languages and contexts.[14]