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 5 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's subclass of is recorded as holoprosencephaly[5].
- Young–Madders syndrome's subclass of is recorded as genetic syndromic intellectual disability[6].
- Young–Madders syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability[7].
- Young–Madders syndrome's MeSH descriptor ID is recorded as C535829[8].
- Young–Madders syndrome's OMIM ID is recorded as 264480[9].
- Young–Madders syndrome's Freebase ID is recorded as /m/0_gzwp1[10].
- Young–Madders syndrome's Orphanet ID is recorded as 2166[11].
- Young–Madders syndrome's NCI Thesaurus ID is recorded as C125418[12].
- Young–Madders syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2166[13].
- Young–Madders syndrome's UMLS CUI is recorded as C1849649[14].
- Young–Madders syndrome's ICD-10-CM is recorded as Q87.8[15].
- Young–Madders syndrome's GARD rare disease ID is recorded as 344[16].
- Young–Madders syndrome's Mondo ID is recorded as MONDO_0009921[17].
Why It Matters
Young–Madders syndrome draws 5 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.[18]