Frasier syndrome

Summary

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

Key Facts

• Frasier syndrome's instance of is recorded as developmental defect during embryogenesis^[2].
• Frasier syndrome's instance of is recorded as rare disease^[3].
• Frasier syndrome's instance of is recorded as class of disease^[4].
• S. Douglas Frasier is named after Frasier syndrome^[5].
• Frasier syndrome is a type of autosomal dominant disease^[6].
• Frasier syndrome is a type of pseudohermaphroditism^[7].
• Frasier syndrome is a type of glomerulopathy^[8].
• Frasier syndrome is a type of syndrome with 46,XY disorder of sex development^[9].
• Frasier syndrome is a type of primary glomerular disease^[10].
• Frasier syndrome is a type of syndrome with disorder of sex development of gynecological interest^[11].
• Frasier syndrome is a type of polymalformative genetic syndrome with increased risk of developing cancer^[12].
• Frasier syndrome is a type of syndrome^[13].
• Frasier syndrome's ICD-9-CM is recorded as 759.89^[14].
• Frasier syndrome's NCI Thesaurus ID is recorded as C122805^[15].
• Frasier syndrome's different from is recorded as Fraser syndrome^[16].
• Frasier syndrome's health specialty is recorded as endocrinology^[17].
• Frasier syndrome's health specialty is recorded as obstetrics and gynaecology^[18].
• Frasier syndrome's health specialty is recorded as urology^[19].
• Frasier syndrome's health specialty is recorded as medical genetics^[20].
• Frasier syndrome's genetic association is recorded as WT1^[21].
• Frasier syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050438^[22].
• Frasier syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050438^[23].
• Frasier syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_347^[24].
• Frasier syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[25].