parietal foramina

Summary

parietal foramina is a hereditary disorder^[1].

Key Facts

• parietal foramina's instance of is recorded as hereditary disorder^[2].
• parietal foramina's instance of is recorded as rare disease^[3].
• parietal foramina's instance of is recorded as class of disease^[4].
• parietal foramina's subclass of is recorded as neural tube defect^[5].
• parietal foramina's MeSH descriptor ID is recorded as C566826^[6].
• parietal foramina's OMIM ID is recorded as 168500^[7].
• parietal foramina's OMIM ID is recorded as 609566^[8].
• parietal foramina's OMIM ID is recorded as 609597^[9].
• parietal foramina's KEGG ID is recorded as H00475^[10].
• parietal foramina's Disease Ontology ID is recorded as DOID:0060285^[11].
• parietal foramina's anatomical location is recorded as Parietal foramen^[12].
• parietal foramina's Orphanet ID is recorded as 60015^[13].
• parietal foramina's genetic association is recorded as MSX2^[14].
• parietal foramina's genetic association is recorded as ALX4^[15].
• parietal foramina's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060285^[16].
• parietal foramina's exact match is recorded as http://identifiers.org/doid/DOID:0060285^[17].
• parietal foramina's exact match is recorded as http://purl.obolibrary.org/obo/HP_0002697^[18].
• parietal foramina's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_60015^[19].
• parietal foramina's UMLS CUI is recorded as C1868598^[20].
• parietal foramina's UMLS CUI is recorded as C0222706^[21].
• parietal foramina's UMLS CUI is recorded as C4280556^[22].
• parietal foramina's Human Phenotype Ontology ID is recorded as HP:0002697^[23].
• parietal foramina's ICD-10-CM is recorded as Q75.8^[24].
• parietal foramina's on focus list of Wikimedia project is recorded as WikiProject Medicine^[25].
• parietal foramina's Mondo ID is recorded as MONDO_0018953^[26].