Phenotypes for disease #01681 (MOPD1 (dwarfism, primordial, osteodysplastic, microcephalic, type 1 (MOPD-1, Taybi-Linder syndrome)), OMIM:210710)

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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     
0000301655 best corrected visual acuity: 1.2; electroretinogram , rod: mildly reduced, cone: mildly reduced - dystrophy, corneoretinal, crystalline, Bietti (BCD) Familial, autosomal recessive 60y - - - - LOVD 00409538
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