Alves syndrome

Summary

Alves syndrome is a hereditary disorder^[1].

Key Facts

• Alves syndrome's instance of is recorded as hereditary disorder^[2].
• Alves syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• Alves syndrome's instance of is recorded as class of disease^[4].
• Alves syndrome's subclass of is recorded as neurogenic arthrogryposis multiplex congenita^[5].
• Alves syndrome's MeSH descriptor ID is recorded as C536593^[6].
• Alves syndrome's OMIM ID is recorded as 601701^[7].
• Alves syndrome's Orphanet ID is recorded as 3354^[8].
• Alves syndrome's Google Knowledge Graph ID is recorded as /g/122mqfjr^[9].
• Alves syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3354^[10].
• Alves syndrome's UMLS CUI is recorded as C1866427^[11].
• Alves syndrome's UMLS CUI is recorded as C2931256^[12].
• Alves syndrome's GARD rare disease ID is recorded as 1553^[13].
• Alves syndrome's Mondo ID is recorded as MONDO_0011131^[14].
• Alves syndrome's ICD-11 ID is recorded as 1206025469^[15].