Phenotypes for disease #00326 (MCOP8 (microphthalmia, isolated, type 8 (MCOP-8)), OMIM:615113)

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000010357 - - - Familial, autosomal recessive - - - - - Daniel Schorderet 00011463
0000016043 - - - Familial, autosomal recessive - - - - - Daniel Schorderet 00017708
0000016044 - - - Familial, autosomal recessive - - - - - Daniel Schorderet 00017709
0000016045 - - - Familial, autosomal recessive - - - - - Daniel Schorderet 00017710
0000016046 - - - Familial, autosomal recessive - - - - - Daniel Schorderet 00017711
0000016047 - - - Familial, autosomal recessive - - - - - Daniel Schorderet 00017712
0000275930 microphthalmia, anophthalmia, and coloboma; MIM, 615113 MIM, 615113 - Familial, autosomal recessive - - - - - LOVD 00382088
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