Phenotypes for disease #01180 (ASGD1 (dysgenesis, anterior segment, type 1 (ASGD1)), OMIM:107250)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000275958 anterior segment developmental anomalies including glaucoma; MIM, 107250 MIM, 107250 - Familial, autosomal dominant - - - - - LOVD 00382116
0000303337 Visual impairment, Abnormal eye morphology, Congenital primary aphakia 1y - Familial, autosomal recessive - - - - - Andreas Laner 00411261
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