Phenotypes for disease #02025 (APBN (polyglucosan body disease, adult (APBN)), OMIM:263570)

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000247313 Proximal myopathy (biopsy proven) Hepatopathy - - Familial, autosomal recessive - - - - - Jonathan De Winter 00329114
0000307090 Leukodystrophy, spinal cord atrophy, peripheral neuropathy, myopathy Adult Polyglucosan Body Disease Adult Polyglucosan Body Disease Familial, autosomal recessive 49y 53y 47y - - Jonathan De Winter 00415292
0000307096 Leukodystrophy, spinal cord atrophy, pure motor axonal neuropathy, myopathy Adult Polyglucosan Body Disease Adult Polyglucosan Body Disease Familial, autosomal recessive 55y 57y 54y 54y - Jonathan De Winter 00415299
0000307099 Leukodystrophy, spinal cord atrophy, sensorimotor peripheral neuropathy Adult Polyglucosan Body Disease Adult Polyglucosan Body Disease Familial, autosomal recessive 72y 73y 67y 67y - Jonathan De Winter 00415302
0000357035 Myopathy, Joint contractures involving the joints of the feet, Sporadic Congenital myopathy - Isolated (sporadic) - - - - - Camille Verebi 00472226
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