Phenotypes for disease #01244 (KFS1 (Klippel-Feil syndrome, type 1, autosomal dominant (KFS1)), OMIM:118100)

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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     
0000275933 microphthalmia, anophthalmia, and coloboma; MIM, 118100 MIM, 118100 - Familial, autosomal dominant - - - - - LOVD 00382091
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