Laurin-Sandrow syndrome
developmental defect during embryogenesis
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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 is a type of syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy[5].
- Laurin-Sandrow syndrome is a type of dysostosis[6].
- Laurin-Sandrow syndrome's genetic association is recorded as SHH[7].
- Laurin-Sandrow syndrome's genetic association is recorded as LMBR1[8].
- Laurin-Sandrow syndrome's exact match is recorded as http://purl.obolibrary.org/obo/HP_0010689[9].
- Laurin-Sandrow syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2378[10].
- Laurin-Sandrow syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111350[11].
- Laurin-Sandrow syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111350[12].