Diaphanospondylodysostosis

Summary

Diaphanospondylodysostosis is a developmental defect during embryogenesis^[1].

Key Facts

• Diaphanospondylodysostosis's instance of is recorded as developmental defect during embryogenesis^[2].
• Diaphanospondylodysostosis's instance of is recorded as rare disease^[3].
• Diaphanospondylodysostosis's instance of is recorded as class of disease^[4].
• Diaphanospondylodysostosis's subclass of is recorded as osteochondrodysplasia^[5].
• Diaphanospondylodysostosis's subclass of is recorded as Spondylodysplastic dysplasia^[6].
• Diaphanospondylodysostosis's subclass of is recorded as dysostosis with predominant vertebral and costal involvement^[7].
• Diaphanospondylodysostosis's MeSH descriptor ID is recorded as C564305^[8].
• Diaphanospondylodysostosis's OMIM ID is recorded as 608022^[9].
• Diaphanospondylodysostosis's ICD-10 ID is recorded as Q78.8^[10].
• Diaphanospondylodysostosis's KEGG ID is recorded as H01844^[11].
• Diaphanospondylodysostosis's Orphanet ID is recorded as 66637^[12].
• Diaphanospondylodysostosis's health specialty is recorded as medical genetics^[13].
• Diaphanospondylodysostosis's genetic association is recorded as BMPER^[14].
• Diaphanospondylodysostosis's Google Knowledge Graph ID is recorded as /g/11clljhggt^[15].
• Diaphanospondylodysostosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_66637^[16].
• Diaphanospondylodysostosis's UMLS CUI is recorded as C1842691^[17].
• Diaphanospondylodysostosis's ICD-10-CM is recorded as Q78.8^[18].
• Diaphanospondylodysostosis's Mondo ID is recorded as MONDO_0011946^[19].
• Diaphanospondylodysostosis's UniProt disease ID is recorded as DI-03157^[20].