Disease #06696 (SPG77 (Spastic paraplegia 77, autosomal recessive), OMIM:617046)

Official abbreviation SPG77
Name Spastic paraplegia 77, autosomal recessive
OMIM ID 617046
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene FARS2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00421533 207860 - - F no Germany - - - - - SPG77 Hypotonia, Motor delay, Lower limb muscle weakness, Impaired pain sensation, Abnormal pyramidal sign, Delayed speech and language development, Joint hypermobility FARS2 FARS2 2 1 Andreas Laner
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