Phenotypes for disease #03396 (KFS3 (Klippel-Feil syndrome, type 3, autosomal dominant (KFS-3)), OMIM:613702)

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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     
0000275932 microphthalmia, anophthalmia, and coloboma; MIM, 613702 MIM, 613702 - Familial, autosomal dominant - - - - - LOVD 00382090
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