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PedAM

Pediatric Disease Annotations & Medicines




Disease tic disorder
Phenotype C0030486|paraplegia
Sentences 2
PubMedID- 22022230 There are genetic links between ap-5 and hereditary spastic paraplegia, a group of human genetic disorders characterised by progressive spasticity in the lower limbs.
PubMedID- 22022232 Identified spg48 as a new gene associated with hereditary spastic paraplegia, a group of genetic disorders characterized by progressive weakness and stiffness of the legs.

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