Phenotypes for disease #04421 (UCMD2 (dystrophy, muscular, congenital, Ullrich, type 2?, (UCMD-2)), OMIM:616470)

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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     
0000345770 IUGR (HP:0001511); joint hypermobility (HP:0001382); frequent falls (HP:0002359); delayed gross motor development (HP:0002194 ); high palate (HP:0000218); distal joint hypermobility (HP:0020152); finger joint contracture (HP:0034681); pes planus (HP:0001763); dry skin (HP:0000958); keratosis pilaris (HP:0032152); limb muscle weakness (HP:0003690). - UCMD2 Familial, autosomal recessive 02y10m 02y10m 00y IUGR (HP:0001511) deepsubs Deepak Subramanian 00457300
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