Phenotypes for disease #01113 (MCCRP1 (microcephaly and chorioretinopathy, autosomal recessive, type 1 (MCCRP-1)), OMIM:251270)

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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

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Individual ID     
0000034209 - - - Familial, autosomal dominant - - - - - Pia Ostergaard 00045114
0000301099 congenital pachygyric microcephaly; global developmental delay; chorioretinopathy and retinal detachment - microcephaly and chorioretinopathy, autosomal recessive, type 1 (MCCRP-1) Familial, autosomal recessive - - - - - LOVD 00408981
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