Laurin-Sandrow syndrome

Summary

Laurin-Sandrow syndrome is a developmental defect during embryogenesis^[1].

Key Facts

• Laurin-Sandrow syndrome's instance of is recorded as developmental defect during embryogenesis^[2].
• Laurin-Sandrow syndrome's instance of is recorded as rare disease^[3].
• Laurin-Sandrow syndrome's instance of is recorded as class of disease^[4].
• Laurin-Sandrow syndrome's subclass of is recorded as syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy^[5].
• Laurin-Sandrow syndrome's subclass of is recorded as dysostosis^[6].
• Laurin-Sandrow syndrome's MeSH descriptor ID is recorded as C535689^[7].
• Laurin-Sandrow syndrome's OMIM ID is recorded as 135750^[8].
• Laurin-Sandrow syndrome's KEGG ID is recorded as H02333^[9].
• Laurin-Sandrow syndrome's Disease Ontology ID is recorded as DOID:0111350^[10].
• Laurin-Sandrow syndrome's Orphanet ID is recorded as 2378^[11].
• Laurin-Sandrow syndrome's genetic association is recorded as SHH^[12].
• Laurin-Sandrow syndrome's genetic association is recorded as LMBR1^[13].
• Laurin-Sandrow syndrome's exact match is recorded as http://purl.obolibrary.org/obo/HP_0010689^[14].
• Laurin-Sandrow syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2378^[15].
• Laurin-Sandrow syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111350^[16].
• Laurin-Sandrow syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111350^[17].
• Laurin-Sandrow syndrome's UMLS CUI is recorded as C1851101^[18].
• Laurin-Sandrow syndrome's UMLS CUI is recorded as C1851100^[19].
• Laurin-Sandrow syndrome's Human Phenotype Ontology ID is recorded as HP:0010689^[20].
• Laurin-Sandrow syndrome's ICD-10-CM is recorded as Q87.2^[21].
• Laurin-Sandrow syndrome's GARD rare disease ID is recorded as 155^[22].
• Laurin-Sandrow syndrome's Mondo ID is recorded as MONDO_0007615^[23].
• Laurin-Sandrow syndrome's UniProt disease ID is recorded as DI-04275^[24].