Meacham syndrome
Meacham syndrome is a multiple malformation syndrome characterized by congenital diaphragmatic abnormalities, genital defects and cardiac malformations
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Meacham syndrome
Summary
Meacham syndrome is a developmental defect during embryogenesis[1].
Key Facts
- Meacham syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- Meacham syndrome's instance of is recorded as rare disease[3].
- Meacham syndrome's instance of is recorded as class of disease[4].
- Meacham syndrome is a type of syndrome with 46,XY disorder of sex development[5].
- Meacham syndrome is a type of syndrome with disorder of sex development of gynecological interest[6].
- Meacham syndrome is a type of syndromic uterovaginal malformation[7].
- Meacham syndrome's genetic association is recorded as WT1[8].
- Meacham syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3097[9].