Phenotypes for disease #01186 (SPAX1 (ataxia, spastic, type 1, autosomal dominant (SPAX-1)), OMIM:108600)

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000041534 ataxia and pyramidal signs lower limbs cerebellar ataxia SCA13 Familial, autosomal dominant - - 01y - - Erik-Jan Kamsteeg 00054870
0000274672 Arthrogryposis; myopathic process (Neurological) - VAMP?1 related disorder Familial - - - - - LOVD 00380819
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.