Phenotypes for disease #04063 (POF8 (ovarian failure, premature, type 8 (POF-8)), OMIM:615723)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000025736 see paper; ...; primary ovarian insufficiency with complete lack of any pubertal development and streak gonads - - Familial, autosomal recessive - - - - - Polona Le Quesne Stabej 00029771
0000025784 see paper - - Familial, autosomal recessive - - - - - Johan den Dunnen 00029856
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