Phenotypes for disease #02380 (ASGD3 (dysgenesis, anterior segment, type 3, multiple subtypes), OMIM:601631)

10 entries on 1 page. Showing entries 1 - 10.
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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     
0000275948 anterior segment developmental anomalies including glaucoma; MIM, 601631 or 602482 MIM, 601631 or 602482 - Familial, autosomal dominant - - - - - LOVD 00382106
0000275949 anterior segment developmental anomalies including glaucoma; MIM, 601631 or 602482 MIM, 601631 or 602482 - Familial, autosomal dominant - - - - - LOVD 00382107
0000275950 anterior segment developmental anomalies including glaucoma; MIM, 601631 or 602482 MIM, 601631 or 602482 - Familial, autosomal dominant - - - - - LOVD 00382108
0000275951 anterior segment developmental anomalies including glaucoma; MIM, 601631 or 602482 MIM, 601631 or 602482 - Familial, autosomal dominant - - - - - LOVD 00382109
0000275952 anterior segment developmental anomalies including glaucoma; MIM, 601631 or 602482 MIM, 601631 or 602482 - Familial, autosomal dominant - - - - - LOVD 00382110
0000275953 anterior segment developmental anomalies including glaucoma; MIM, 601631 or 602482 MIM, 601631 or 602482 - Familial, autosomal dominant - - - - - LOVD 00382111
0000275954 anterior segment developmental anomalies including glaucoma; MIM, 601631 or 602482 MIM, 601631 or 602482 - Familial, autosomal dominant - - - - - LOVD 00382112
0000275955 anterior segment developmental anomalies including glaucoma; MIM, 601631 or 602482 MIM, 601631 or 602482 - Familial, autosomal dominant - - - - - LOVD 00382113
0000275956 anterior segment developmental anomalies including glaucoma; MIM, 601631 or 602482 MIM, 601631 or 602482 - Familial, autosomal dominant - - - - - LOVD 00382114
0000275957 anterior segment developmental anomalies including glaucoma; MIM, 601631 or 602482 MIM, 601631 or 602482 - Familial, autosomal dominant - - - - - LOVD 00382115
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