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Disease Larsen-Like Syndrome

Name Larsen-Like Syndrome
Synonym LRSL
Categories Congenital abnormality | Genetic disease (inborn) | Musculoskeletal disease | Pathology (process) | Wounds and injuries
MeSH® ID C563914
OMIM® ID 608545

Top ↑ Ancestors

1. DiseasesMusculoskeletal Diseases Has associated chemicals Has associated genes Has associated exposure references Bone Diseases Has associated chemicals Has associated genes Has associated exposure references Bone Diseases, Developmental Has associated chemicals Has associated genes Osteochondrodysplasias Has associated chemicals Has associated genes Larsen-Like Syndrome Has associated genes
2. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Congenital Abnormalities Has associated chemicals Has associated genes Has associated exposure references Abnormalities, Multiple Has associated chemicals Has associated genes Larsen-Like Syndrome Has associated genes
3. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Osteochondrodysplasias Has associated chemicals Has associated genes Larsen-Like Syndrome Has associated genes
4. DiseasesPathological Conditions, Signs and Symptoms Has associated chemicals Has associated genes Has associated exposure references Pathologic Processes Has associated chemicals Has associated genes Has associated exposure references Disease Attributes Has associated chemicals Has associated genes Has associated exposure references Facies Has associated chemicals Has associated genes Larsen-Like Syndrome Has associated genes
5. DiseasesWounds and Injuries Has associated chemicals Has associated genes Has associated exposure references Dislocations Has associated chemicals Has associated genes Larsen-Like Syndrome Has associated genes

Top ↑ Descendants

None.