Rienhoff syndrome

Summary

Rienhoff syndrome is a rare disease^[1].

Key Facts

• Rienhoff syndrome's instance of is recorded as rare disease^[2].
• Rienhoff syndrome's instance of is recorded as class of disease^[3].
• Rienhoff syndrome's subclass of is recorded as Loeys-Dietz syndrome^[4].
• Rienhoff syndrome's OMIM ID is recorded as 615582^[5].
• Rienhoff syndrome's KEGG ID is recorded as H01385^[6].
• Rienhoff syndrome's Disease Ontology ID is recorded as DOID:0070236^[7].
• Rienhoff syndrome's NCI Thesaurus ID is recorded as C188143^[8].
• Rienhoff syndrome's genetic association is recorded as TGFB3^[9].
• Rienhoff syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070236^[10].
• Rienhoff syndrome's UMLS CUI is recorded as C3810012^[11].
• Rienhoff syndrome's GARD rare disease ID is recorded as 12356^[12].
• Rienhoff syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[13].
• Rienhoff syndrome's Mondo ID is recorded as MONDO_0014262^[14].
• Rienhoff syndrome's UniProt disease ID is recorded as DI-03991^[15].
• Rienhoff syndrome's Experimental Factor Ontology ID is recorded as 1000012^[16].