Regulation of Transcription Ontology

Last uploaded: December 4, 2018
Preferred Name

Spastic paraplegia 39, autosomal recessive
Synonyms

SPG39

Definitions

(SPG39) - A form of spastic paraplegia, a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. SPG39 is associated with a motor axonopathy affecting upper and lower limbs and resulting in progressive wasting of distal upper and lower extremity muscles.

ID

http://identifiers.org/omim/612020

altLabel

SPG39

definition

(SPG39) - A form of spastic paraplegia, a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. SPG39 is associated with a motor axonopathy affecting upper and lower limbs and resulting in progressive wasting of distal upper and lower extremity muscles.

id

OMIM:612020

notation

OMIM:612020

prefLabel

Spastic paraplegia 39, autosomal recessive

subClassOf

http://purl.obolibrary.org/obo/OGMS_0000031

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