Skip navigation

Disease Spastic paraplegia 13, autosomal dominant

Name Spastic paraplegia 13, autosomal dominant
Synonym SPG13
Categories Congenital abnormality | Genetic disease (inborn) | Nervous system disease
MeSH® ID C537485
OMIM® ID 605280

Top ↑ Ancestors

1. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Nervous System Malformations Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Hereditary Sensory and Motor Neuropathy Has associated chemicals Has associated genes Has associated phenotype references Spastic Paraplegia, Hereditary Has associated chemicals Has associated genes Has associated phenotype references Spastic paraplegia 13, autosomal dominant Has associated chemicals Has associated genes Has associated phenotype references
2. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Neurodegenerative Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Heredodegenerative Disorders, Nervous System Has associated chemicals Has associated genes Has associated phenotype references Hereditary Sensory and Motor Neuropathy Has associated chemicals Has associated genes Has associated phenotype references Spastic Paraplegia, Hereditary Has associated chemicals Has associated genes Has associated phenotype references Spastic paraplegia 13, autosomal dominant Has associated chemicals Has associated genes Has associated phenotype references
3. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Neuromuscular Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Peripheral Nervous System Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Polyneuropathies Has associated chemicals Has associated genes Has associated phenotype references Hereditary Sensory and Motor Neuropathy Has associated chemicals Has associated genes Has associated phenotype references Spastic Paraplegia, Hereditary Has associated chemicals Has associated genes Has associated phenotype references Spastic paraplegia 13, autosomal dominant Has associated chemicals Has associated genes Has associated phenotype references
4. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Congenital Abnormalities Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Nervous System Malformations Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Hereditary Sensory and Motor Neuropathy Has associated chemicals Has associated genes Has associated phenotype references Spastic Paraplegia, Hereditary Has associated chemicals Has associated genes Has associated phenotype references Spastic paraplegia 13, autosomal dominant Has associated chemicals Has associated genes Has associated phenotype references
5. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Heredodegenerative Disorders, Nervous System Has associated chemicals Has associated genes Has associated phenotype references Hereditary Sensory and Motor Neuropathy Has associated chemicals Has associated genes Has associated phenotype references Spastic Paraplegia, Hereditary Has associated chemicals Has associated genes Has associated phenotype references Spastic paraplegia 13, autosomal dominant Has associated chemicals Has associated genes Has associated phenotype references

Top ↑ Descendants

None.