Phenotypes for disease #01775 (EBSMD (epidermolysa bullosa simplex, with muscular dystrophy (EBSMD)), OMIM:226670)

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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     
0000300414 Cutaneous: skin blistering, nail dystrophy, alopecia Oropharyngeal: enamel hypoplasia, hoarseness, recurrent choking, required laryngotomy at age 7 due to ulcer in larynx Musculoskeletal: Proximal muscle weakness: 4 out of 5, distal muscle weakness: 4 out of 5, ptosis (left worse than right) Respiratory: admissions due to respiratory problems Cardiac: None - - Familial, autosomal recessive 15y - - - - Nailah Harvey 00408289
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