Boylan Dew Greco syndrome

Summary

Boylan Dew Greco syndrome is a rare disease^[1].

Key Facts

• Boylan Dew Greco syndrome's instance of is recorded as rare disease^[2].
• Boylan Dew Greco syndrome's instance of is recorded as class of disease^[3].
• Boylan Dew Greco syndrome's subclass of is recorded as nervous system heredodegenerative disease^[4].
• Boylan Dew Greco syndrome's subclass of is recorded as demyelinating disease^[5].
• Boylan Dew Greco syndrome's subclass of is recorded as arthrogryposis^[6].
• Boylan Dew Greco syndrome's subclass of is recorded as rare genetic developmental defect during embryogenesis^[7].
• Boylan Dew Greco syndrome's MeSH descriptor ID is recorded as C537083^[8].
• Boylan Dew Greco syndrome's Orphanet ID is recorded as 2680^[9].
• Boylan Dew Greco syndrome's genetic association is recorded as CNTNAP1^[10].
• Boylan Dew Greco syndrome's genetic association is recorded as ADCY6^[11].
• Boylan Dew Greco syndrome's Google Knowledge Graph ID is recorded as /g/11j13yt_pr^[12].
• Boylan Dew Greco syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2680^[13].
• Boylan Dew Greco syndrome's UMLS CUI is recorded as C2931419^[14].
• Boylan Dew Greco syndrome's UMLS CUI is recorded as C4707882^[15].
• Boylan Dew Greco syndrome's GARD rare disease ID is recorded as 954^[16].
• Boylan Dew Greco syndrome's Mondo ID is recorded as MONDO_0022025^[17].