CODAS syndrome

Summary

CODAS syndrome is a developmental defect during embryogenesis^[1]. It is known by 7 alternative names across languages and contexts.^[2]

Key Facts

• CODAS syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• CODAS syndrome's instance of is recorded as rare disease^[4].
• CODAS syndrome's instance of is recorded as class of disease^[5].
• CODAS syndrome is a type of rare genetic developmental defect during embryogenesis^[6].
• CODAS syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability^[7].
• CODAS syndrome is a type of syndrome^[8].
• CODAS syndrome is a type of autosomal recessive disease^[9].
• CODAS syndrome's NCI Thesaurus ID is recorded as C126744^[10].
• CODAS syndrome's genetic association is recorded as LONP1^[11].
• CODAS syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1458^[12].
• CODAS syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111274^[13].
• CODAS syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111274^[14].

Why It Matters

CODAS syndrome is known by 7 alternative names across languages and contexts.^[2]