heart-hand syndrome, Slovenian type
medical condition
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heart-hand syndrome, Slovenian type
Summary
heart-hand syndrome, Slovenian type is a developmental defect during embryogenesis[1]. It draws 3 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).[2]
Key Facts
- heart-hand syndrome, Slovenian type's instance of is recorded as developmental defect during embryogenesis[3].
- heart-hand syndrome, Slovenian type's instance of is recorded as rare disease[4].
- heart-hand syndrome, Slovenian type's instance of is recorded as class of disease[5].
- heart-hand syndrome, Slovenian type's subclass of is recorded as Holt-Oram syndrome[6].
- heart-hand syndrome, Slovenian type's subclass of is recorded as syndrome associated with dilated cardiomyopathy[7].
- heart-hand syndrome, Slovenian type's MeSH descriptor ID is recorded as C535852[8].
- heart-hand syndrome, Slovenian type's OMIM ID is recorded as 610140[9].
- heart-hand syndrome, Slovenian type's Orphanet ID is recorded as 168796[10].
- heart-hand syndrome, Slovenian type's genetic association is recorded as LMNA[11].
- heart-hand syndrome, Slovenian type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_168796[12].
- heart-hand syndrome, Slovenian type's UMLS CUI is recorded as C1857829[13].
- heart-hand syndrome, Slovenian type's ICD-10-CM is recorded as Q87.2[14].
- heart-hand syndrome, Slovenian type's GARD rare disease ID is recorded as 9846[15].
- heart-hand syndrome, Slovenian type's Mondo ID is recorded as MONDO_0012417[16].
- heart-hand syndrome, Slovenian type's UniProt disease ID is recorded as DI-01697[17].
Why It Matters
heart-hand syndrome, Slovenian type draws 3 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).[2]