Phenotypes for disease #01932 (ML4 (Mucolipidosis IV), OMIM:252650)

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AscendingPhenotype ID     

Phenotype details     

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Age/Diagnosis     

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Owner     

Individual ID     
0000351835 Vitreoretinopathy, Delayed speech and language development, Hearing impairment, Hypotonia, Motor delay, achlorhydria, anaemia, Motor delay and strabism Mucolipidosis IV Familial, autosomal recessive 1y 8 months 03y 1y 8 months Chilhood onset - Maria Elena García Paya 00466473
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