Peters plus syndrome

Summary

Peters plus syndrome is a rare disease^[1]. It draws 10 Wikipedia views per month (rare_disease category, ranking #234 of 627).^[2]

Key Facts

• Peters plus syndrome's instance of is recorded as rare disease^[3].
• Peters plus syndrome's instance of is recorded as developmental defect during embryogenesis^[4].
• Peters plus syndrome's instance of is recorded as class of disease^[5].
• Peters plus syndrome is a type of syndrome^[6].
• Peters plus syndrome is a type of syndromic developmental defect of the eye^[7].
• Peters plus syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability^[8].
• Peters plus syndrome is a type of congenital disorder of glycosylation with cardiac malformation as a major feature^[9].
• Peters plus syndrome is a type of non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature^[10].
• Peters plus syndrome is a type of disorder of fucoglycosan synthesis^[11].
• Peters plus syndrome is a type of syndromic glaucoma^[12].
• Peters plus syndrome's symptoms and signs is recorded as anterior segment mesenchymal dysgenesis^[13].
• Peters plus syndrome's ICD-9-CM is recorded as 743.44^[14].
• Peters plus syndrome's NCI Thesaurus ID is recorded as C123436^[15].
• Peters plus syndrome's genetic association is recorded as B3GLCT^[16].
• Peters plus syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080201^[17].
• Peters plus syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080201^[18].
• Peters plus syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_709^[19].
• Peters plus syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[20].

Why It Matters

Peters plus syndrome draws 10 Wikipedia views per month (rare_disease category, ranking #234 of 627).^[2]