Phenotypes for disease #01945 (UCMD (dystrophy, muscular, congenital, Ullrich))

7 entries on 1 page. Showing entries 1 - 7.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000060428 Ullrich congenital muscular dystrophy 1 (OMIM:254090) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080859
0000060462 Ullrich congenital muscular dystrophy 1 (OMIM:254090) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080893
0000060663 Ullrich congenital muscular dystrophy 1 (OMIM:254090) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081094
0000086889 progressive weakness, distal finger hyperlaxity, contractures of elbows, knees/ankles, mild scoliosis, mild keratosis pilaris; wheelchair-bound teens; FVC 0.31 - - Familial, autosomal dominant - 24y - - - Sandra Donkervoort 00109416
0000086890 delayed motor mile stones, proximal weakness, distal finger hyperlaxity with coexisting and long finger flexor contractures: limited shoulder abduction; rigid spine, keratosis pilaris, keloid scarring; FVC 0.83 - - Familial, autosomal dominant - - - - - Sandra Donkervoort 00109417
0000086891 congenital arthrogryposis, bilateral hip dislocation; severe proximal weakness, distal finger hyperlaxity with long finger contractures; rigid spine; FVC 0.30 - - Familial, autosomal dominant - - - - - Sandra Donkervoort 00109418
0000173142 Motor delay (HP:0001270); Proximal muscle weakness (HP:0003701); Joint laxity (HP:0001388); Generalised hypotonia (HP:0001290); Hyperextensibility of wrists (HP:0005072); Elevated serum creatine kinase (HP:0003236); EMG:myopathic abnormalities (HP:0003458); Talipes equinovarus (HP:0001762); no follicular hyperkeratosis (-HP:0007502); no flexion contracture (-HP:0001371) - Ullrich congenital muscular dystrophy-1 Familial, autosomal recessive 11y 11y 02y - - Nirmala Sirisena 00230584
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