Curry-Jones syndrome

Summary

Curry-Jones syndrome is a developmental defect during embryogenesis^[1]. It draws 2 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).^[2]

Key Facts

• Curry-Jones syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• Curry-Jones syndrome's instance of is recorded as class of disease^[4].
• Curry-Jones syndrome's subclass of is recorded as genetic nervous system disorder^[5].
• Curry-Jones syndrome's subclass of is recorded as syndrome with corpus callosum agenesis /dysgenesis as a major feature^[6].
• Curry-Jones syndrome's subclass of is recorded as syndromic craniosynostosis^[7].
• Curry-Jones syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome^[8].
• Curry-Jones syndrome's OMIM ID is recorded as 601707^[9].
• Curry-Jones syndrome's Orphanet ID is recorded as 1553^[10].
• Curry-Jones syndrome's genetic association is recorded as SMO^[11].
• Curry-Jones syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1553^[12].
• Curry-Jones syndrome's UMLS CUI is recorded as C0795915^[13].
• Curry-Jones syndrome's ICD-10-CM is recorded as Q87.0^[14].
• Curry-Jones syndrome's GARD rare disease ID is recorded as 5584^[15].
• Curry-Jones syndrome's Mondo ID is recorded as MONDO_0011134^[16].
• Curry-Jones syndrome's UniProt disease ID is recorded as DI-04790^[17].

Why It Matters

Curry-Jones syndrome draws 2 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).^[2]