dipygus
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dipygus
Summary
dipygus is a developmental defect during embryogenesis[1]. dipygus has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- dipygus's instance of is recorded as developmental defect during embryogenesis[3].
- dipygus's instance of is recorded as rare disease[4].
- dipygus's instance of is recorded as class of disease[5].
- dipygus is a type of genetic nervous system disorder[6].
- dipygus is a type of other syndrome with a central nervous system malformation as major feature[7].
- dipygus is a type of syndromic anorectal malformation[8].
- dipygus is a type of Caudal duplication[9].
- dipygus's genetic association is recorded as AXIN1[10].
- dipygus's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1756[11].
Why It Matters
dipygus has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] dipygus is known by 5 alternative names across languages and contexts.[12]