RIN2 syndrome

Summary

RIN2 syndrome is a developmental defect during embryogenesis^[1].

Key Facts

• RIN2 syndrome's instance of is recorded as developmental defect during embryogenesis^[2].
• RIN2 syndrome's instance of is recorded as rare disease^[3].
• RIN2 syndrome's instance of is recorded as class of disease^[4].
• RIN2 syndrome's subclass of is recorded as disease^[5].
• RIN2 syndrome's MeSH descriptor ID is recorded as C567770^[6].
• RIN2 syndrome's OMIM ID is recorded as 613075^[7].
• RIN2 syndrome's KEGG ID is recorded as H00906^[8].
• RIN2 syndrome's Orphanet ID is recorded as 217335^[9].
• RIN2 syndrome's genetic association is recorded as RIN2^[10].
• RIN2 syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_217335^[11].
• RIN2 syndrome's UMLS CUI is recorded as C2751321^[12].
• RIN2 syndrome's ICD-10-CM is recorded as Q82.8^[13].
• RIN2 syndrome's Mondo ID is recorded as MONDO_0013115^[14].
• RIN2 syndrome's ICD-11 ID is recorded as 648412341^[15].
• RIN2 syndrome's UniProt disease ID is recorded as DI-02637^[16].