Phenotypes for disease #02952 (PPROM (preterm premature rupture of membranes (PPROM)), OMIM:610504)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000326739 Photophobia HP:0000613, Reduced visual acuity HP:0007663, Large central visual field defect HP:0001129, Color vision defect HP: 0000551 Retinal dystrophy # 608051 Familial, autosomal recessive 03y 30y 03y 3y - Rocio Villafuerte-de la Cruz 00436589
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