Phenotypes for disease #00075 (MKS3 (Meckel syndrome, type 3), OMIM:607361)

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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

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Owner     

Individual ID     
0000070577 - Familial, autosomal recessive - - - - - mild IDD, adolescent-onset dementia, vertical gaze palsy, ataxia, ADHD, cerebellar atrophy at age 8y (molar tooth sign at age 22y, after diagnosis established), hepatosplenomegaly,progressive hepatic fibrosis, portal hypertension,; lysosomal storage disease phenotype - Johan den Dunnen 00092243
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