Meacham syndrome

Summary

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

Key Facts

• Meacham syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• Meacham syndrome's instance of is recorded as rare disease^[4].
• Meacham syndrome's instance of is recorded as class of disease^[5].
• Meacham syndrome's subclass of is recorded as syndrome with 46,XY disorder of sex development^[6].
• Meacham syndrome's subclass of is recorded as syndrome with disorder of sex development of gynecological interest^[7].
• Meacham syndrome's subclass of is recorded as syndromic uterovaginal malformation^[8].
• Meacham syndrome's OMIM ID is recorded as 608978^[9].
• Meacham syndrome's Orphanet ID is recorded as 3097^[10].
• Meacham syndrome's genetic association is recorded as WT1^[11].
• Meacham syndrome's Google Knowledge Graph ID is recorded as /g/11f6151_4l^[12].
• Meacham syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3097^[13].
• Meacham syndrome's UMLS CUI is recorded as C1837026^[14].
• Meacham syndrome's UMLS CUI is recorded as C2931752^[15].
• Meacham syndrome's ICD-10-CM is recorded as Q87.8^[16].
• Meacham syndrome's GARD rare disease ID is recorded as 3432^[17].
• Meacham syndrome's Mondo ID is recorded as MONDO_0012164^[18].
• Meacham syndrome's UniProt disease ID is recorded as DI-01955^[19].

Why It Matters

Meacham syndrome draws 1 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).^[2]