hypoplasminogenemia
medical condition
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hypoplasminogenemia
Summary
hypoplasminogenemia is a class of disease[1].
Key Facts
- hypoplasminogenemia's instance of is recorded as class of disease[2].
- hypoplasminogenemia's subclass of is recorded as coagulation protein disease[3].
- hypoplasminogenemia's MeSH descriptor ID is recorded as C580017[4].
- hypoplasminogenemia's OMIM ID is recorded as 217090[5].
- hypoplasminogenemia's KEGG ID is recorded as H01206[6].
- hypoplasminogenemia's Orphanet ID is recorded as 722[7].
- hypoplasminogenemia's genetic association is recorded as PLG[8].
- hypoplasminogenemia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_722[9].
- hypoplasminogenemia's UMLS CUI is recorded as C1968804[10].
- hypoplasminogenemia's UMLS CUI is recorded as C0398621[11].
- hypoplasminogenemia's ICD-10-CM is recorded as L90.5[12].
- hypoplasminogenemia's Mondo ID is recorded as MONDO_0009009[13].
- hypoplasminogenemia's ICD-11 ID is recorded as DA0D.3[14].
- hypoplasminogenemia's ICD-11 ID is recorded as 1240776230[15].
- hypoplasminogenemia's UniProt disease ID is recorded as DI-02666[16].