Peters plus syndrome
syndrome that is characterized by anterior chamber eye anomalies, short limbs with broad distal extremities, characteristic facial features, cleft lip/palate, and variable developmental delay/intellectual disability
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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's subclass of is recorded as syndrome[6].
- Peters plus syndrome's subclass of is recorded as syndromic developmental defect of the eye[7].
- Peters plus syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability[8].
- Peters plus syndrome's subclass of is recorded as congenital disorder of glycosylation with cardiac malformation as a major feature[9].
- Peters plus syndrome's subclass of is recorded as non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature[10].
- Peters plus syndrome's subclass of is recorded as disorder of fucoglycosan synthesis[11].
- Peters plus syndrome's subclass of is recorded as syndromic glaucoma[12].
- Peters plus syndrome's MeSH descriptor ID is recorded as C537617[13].
- Peters plus syndrome's OMIM ID is recorded as 261540[14].
- Peters plus syndrome's Disease Ontology ID is recorded as DOID:0080201[15].
- Peters plus syndrome's symptoms and signs is recorded as anterior segment mesenchymal dysgenesis[16].
- Peters plus syndrome's Orphanet ID is recorded as 709[17].
- Peters plus syndrome's ICD-9-CM is recorded as 743.44[18].
- Peters plus syndrome's NCI Thesaurus ID is recorded as C123436[19].
- Peters plus syndrome's genetic association is recorded as B3GLCT[20].
- Peters plus syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080201[21].
- Peters plus syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080201[22].
- Peters plus syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_709[23].
- Peters plus syndrome's UMLS CUI is recorded as C0796012[24].
- Peters plus syndrome's ICD-10-CM is recorded as Q13.4[25].
- Peters plus syndrome's GARD rare disease ID is recorded as 8422[26].
- Peters plus syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].
Why It Matters
Peters plus syndrome draws 10 Wikipedia views per month (rare_disease category, ranking #234 of 627).[2]