Phenotypes for disease #01266 (EBMD (dystrophy, corneal, epithelial basement membrane (EBMD)), OMIM:121820)

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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     
0000300417 Cutaneous: skin blistering Oropharyngeal: dental caries, hoarseness Musculoskeletal: Proximal muscle weakness: 4 out of 5, distal muscle weakness: 4 out of 5, ptosis, lower limbs spasticity, severe motor delay: sitting at age 2.5, speech delay - - Familial, autosomal recessive - - - - - Nailah Harvey 00408291
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