progenism

Summary

progenism is a developmental defect during embryogenesis^[1].

Key Facts

• progenism's instance of is recorded as developmental defect during embryogenesis^[2].
• progenism's instance of is recorded as class of disease^[3].
• progenism's subclass of is recorded as malocclusion^[4].
• progenism's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome without intellectual disability^[5].
• progenism's subclass of is recorded as rare genetic developmental defect during embryogenesis^[6].
• progenism's subclass of is recorded as prognathism^[7].
• progenism's MeSH descriptor ID is recorded as D008313^[8].
• progenism's OMIM ID is recorded as 176700^[9].
• progenism's BNCF Thesaurus ID is recorded as 24482^[10].
• progenism's MeSH tree code is recorded as C07.793.494.650^[11].
• progenism's Orphanet ID is recorded as 2964^[12].
• progenism's health specialty is recorded as oral and maxillofacial surgery^[13].
• progenism's health specialty is recorded as orthodontics^[14].
• progenism's exact match is recorded as http://purl.obolibrary.org/obo/HP_0000303^[15].
• progenism's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2964^[16].
• progenism's UMLS CUI is recorded as C0266075^[17].
• progenism's UMLS CUI is recorded as C0399526^[18].
• progenism's UMLS CUI is recorded as C4280645^[19].
• progenism's UMLS CUI is recorded as C0302501^[20].
• progenism's UMLS CUI is recorded as C2227134^[21].
• progenism's UMLS CUI is recorded as C4280644^[22].
• progenism's UMLS CUI is recorded as C5680744^[23].
• progenism's Human Phenotype Ontology ID is recorded as HP:0000303^[24].
• progenism's ICD-10-CM is recorded as K07.1^[25].
• progenism's Mondo ID is recorded as MONDO_0008312^[26].