Phenotypes for disease #00775 (OCRL (Lowe oculocerebrorenal syndrome (OCRL)), OMIM:309000)

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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     
0000186534 - - - Familial - - - - - Xia Zhang 00246689
0000296462 born at term; normal motor milestones; delayed speech and language; 3y-short stature, bilateral cataracts ; 5y-acute and chronic renal failure after 3w episode of vomiting, headaches, weight loss Lowe syndrome OCRL Familial, X-linked recessive 05y - - - - Johan den Dunnen 00403763
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