facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation
human disease
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Summary
facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation is a developmental defect during embryogenesis[1]. It draws 427 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #118 of 308).[2]
Key Facts
- facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation's instance of is recorded as developmental defect during embryogenesis[3].
- facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation's instance of is recorded as rare disease[4].
- facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation's instance of is recorded as class of disease[5].
- facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation is a type of syndromic intellectual disability[6].
- facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation is a type of partial deletion of the short arm of chromosome 10[7].
- facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation's genetic association is recorded as WAC[8].
- facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_466950[9].
Why It Matters
facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation draws 427 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #118 of 308).[2] It is known by 5 alternative names across languages and contexts.[10]