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Disease Spondyloepimetaphyseal dysplasia with hypotrichosis

Name Spondyloepimetaphyseal dysplasia with hypotrichosis
Synonyms Whyte Petersen McAlister syndrome | Whyte syndrome
Categories Genetic disease (inborn) | Musculoskeletal disease | Skin disease
MeSH® ID C535783

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 Spondyloepimetaphyseal dysplasia with hypotrichosis
2. 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 Spondyloepimetaphyseal dysplasia with hypotrichosis
3. DiseasesSkin and Connective Tissue Diseases Has associated chemicals Has associated genes Has associated exposure references Skin Diseases Has associated chemicals Has associated genes Has associated exposure references Hair Diseases Has associated chemicals Has associated genes Hypotrichosis Has associated chemicals Has associated genes Spondyloepimetaphyseal dysplasia with hypotrichosis

Top ↑ Descendants

None.