Phenotypes for disease #02071 (sialuria (sialuria, French type), OMIM:269921)

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     
0000042705 moderate developmental delay, hepatosplenomegaly, slightly coarse facial features, large tongue, macrocephaly, massive urinary excretion free sialic acid; 7y-mild intellectual impairment (attends regular school), fine-motor difficulty, growth 10th percentile, organomegaly persistent - - Unknown - - 2y - - Johan den Dunnen 00056067
0000042706 hepatomegaly, dysmorphic facies, hirsutism, normal growth; 6y-IQ68; - - Unknown - - 4y6m - - Johan den Dunnen 00056068
0000042707 hepatomegaly, coarse voice, facial features; 5y-growth/development normal; - - Unknown - - 10m - - Johan den Dunnen 00056069
0000042708 sialuria - - Unknown - - 28m - - Johan den Dunnen 00056070
0000042738 sialuria; - - Unknown - - - - - Johan den Dunnen 00056100
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