Young–Madders syndrome
Holoprosencephaly-postaxial polydactyly syndrome associates, in chromosomally normal neonates, holoprosencephaly, severe facial dysmorphism, postaxial polydactyly and other congenital abnormalities, suggestive of trisomy 13 (see this term)
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Young–Madders syndrome
Summary
Young–Madders syndrome is a developmental defect during embryogenesis[1]. It draws 70 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #131 of 308).[2]
Key Facts
- Young–Madders syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Young–Madders syndrome's instance of is recorded as class of disease[4].
- Young–Madders syndrome is a type of holoprosencephaly[5].
- Young–Madders syndrome is a type of genetic syndromic intellectual disability[6].
- Young–Madders syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[7].
- Young–Madders syndrome's NCI Thesaurus ID is recorded as C125418[8].
- Young–Madders syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2166[9].
Why It Matters
Young–Madders syndrome draws 70 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #131 of 308).[2] It is known by 6 alternative names across languages and contexts.[10]