Phenotypes for disease #00215 (KRS;CLN12;PARK9 (Kufor-Rakeb syndrome), OMIM:606693)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000001866 hereditary spastic paraplegia, Parkinson disease, ID, slow vertical saccades hereditary spastic paraplegia PARK9 Isolated (sporadic) - - <01y - - Marcel Nelen 00003015
0000080879 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00102746
0000080880 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00102747
0000233300 Visual impairment, Retinal dystrophy, Seizures, Muscular hypotonia, Global developmental delay, Brisk reflexes, Hepatomegaly, Exaggerated startle response, Elevated hepatic transaminase, Mongolian blue spot, Brain atrophy, Abnormal myelination - - Familial, autosomal recessive - 02y09m ? - - Corina-Marcela Rus 00307875
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