Phenotypes for disease #05050 (CFEOM3A (fibrosis of extraocular muscles, congenital, type 3A (CFEOM-3A)), OMIM:600638)

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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     
0000078646 Aplasia/Hypoplasia of the corpus callosum;Abnormality of olfactory lobe morphology; Abnormality of the seventh cranial nerve; abnormality of the cranial nerve;neurodevelopmental delay;facial diplegia;intellectual disability, moderate;ptosis;strabismus;nistagmus;dysmorphic facies - - Isolated (sporadic) - - - - - Enza Maria Valente 00100445
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