Phenotypes for disease #01053 (HH1;KAL1 (hypogonadism, hypogonadotropic, type 1, with/without anosmia (Kallmann syndrome)), OMIM:308700)

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     
0000028306 hypogonadotropic hypogonadism, anosmia or hyposmia, no mental retardation - - Familial, X-linked recessive 29y - - - - Fei Wang 00037755
0000028308 hypogonatropic hypogonadism, anosmy, cryptorchidism - - Unknown 13y - - - - Cecile Libioulle 00037757
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