Phenotypes for disease #04171 (STRMK (Stormorken syndrome (STRMK)), OMIM:185070)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000025032 see paper; congenital miosis, bleeding diathesis, thrombocytopenia, proximal muscle weakness - - Isolated (sporadic) - - - - - Johan den Dunnen 00029011
0000025033 see paper; congenital miosis, bleeding diathesis, thrombocytopenia, proximal muscle weakness - - Unknown - - - - - Johan den Dunnen 00029012
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