CAMOS syndrome

Summary

CAMOS syndrome is a developmental defect during embryogenesis^[1].

Key Facts

• CAMOS syndrome's instance of is recorded as developmental defect during embryogenesis^[2].
• CAMOS syndrome's instance of is recorded as class of disease^[3].
• CAMOS syndrome's subclass of is recorded as autosomal recessive congenital cerebellar ataxia^[4].
• CAMOS syndrome's subclass of is recorded as syndromic hereditary optic neuropathy^[5].
• CAMOS syndrome's OMIM ID is recorded as 606937^[6].
• CAMOS syndrome's Orphanet ID is recorded as 83472^[7].
• CAMOS syndrome's genetic association is recorded as WDR73^[8].
• CAMOS syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_83472^[9].
• CAMOS syndrome's UMLS CUI is recorded as C1847114^[10].
• CAMOS syndrome's UMLS CUI is recorded as C4511633^[11].
• CAMOS syndrome's ICD-10-CM is recorded as G11.1^[12].
• CAMOS syndrome's GARD rare disease ID is recorded as 9977^[13].
• CAMOS syndrome's Mondo ID is recorded as MONDO_0019374^[14].