Phenotypes for disease #01715 (ACHM2 (achromatopsia, type 2 (ACHM-2)), OMIM:216900)

5 entries on 1 page. Showing entries 1 - 5.
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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     
0000275929 microphthalmia, anophthalmia, and coloboma; MIM, 206920 MIM, 206920 - Familial, autosomal recessive - - - - - LOVD 00382087
0000275965 retinal dystrophy; MIM, 216900 MIM, 216900 - Familial, autosomal recessive - - - - - LOVD 00382123
0000275966 retinal dystrophy; MIM, 216900 MIM, 216900 - Familial, autosomal recessive - - - - - LOVD 00382124
0000275967 retinal dystrophy; MIM, 216900 MIM, 216900 - Familial, autosomal recessive - - - - - LOVD 00382125
0000275968 retinal dystrophy; MIM, 216900 MIM, 216900 - Familial, autosomal recessive - - - - - LOVD 00382126
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