epiblepharon
human disease
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epiblepharon
Summary
epiblepharon is a class of disease[1].
Key Facts
- epiblepharon's instance of is recorded as class of disease[2].
- epiblepharon's subclass of is recorded as congenital physical abnormality[3].
- epiblepharon's subclass of is recorded as eyelids malposition disorder[4].
- epiblepharon's MeSH descriptor ID is recorded as C565051[5].
- epiblepharon's OMIM ID is recorded as 131450[6].
- epiblepharon's ICD-10 ID is recorded as Q10.3[7].
- epiblepharon's anatomical location is recorded as eyelid[8].
- epiblepharon's Orphanet ID is recorded as 99169[9].
- epiblepharon's ICD-9-CM is recorded as 743.63[10].
- epiblepharon's health specialty is recorded as medical genetics[11].
- epiblepharon's exact match is recorded as http://purl.obolibrary.org/obo/HP_0040150[12].
- epiblepharon's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99169[13].
- epiblepharon's UMLS CUI is recorded as C0344503[14].
- epiblepharon's UMLS CUI is recorded as C1851582[15].
- epiblepharon's Human Phenotype Ontology ID is recorded as HP:0040150[16].
- epiblepharon's ICD-10-CM is recorded as Q10.3[17].
- epiblepharon's Store medisinske leksikon ID is recorded as epiblefaron[18].
- epiblepharon's Mondo ID is recorded as MONDO_0020461[19].
- epiblepharon's Microsoft Academic ID is recorded as 2776602772[20].
- epiblepharon's ICD-11 ID is recorded as 1757021264[21].