Phenotypes for disease #01710 (GRBGD (Greenberg skeletal dysplasia), OMIM:215140)

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AscendingPhenotype ID     

Phenotype details     

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Owner     

Individual ID     
0000324780 Abnormality of prenatal development or birth, Skeletal dysplasia, Thickened nuchal skin fold, Micromelia, Postaxial polydactyly, Abnormal thorax morphology, Single umbilical artery - - Familial, autosomal recessive 13+5 - - - - Andreas Laner 00434444
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