Phenotypes for disease #01388 (HH7 (hypogonadism, hypogonadotropic, type 7 (HH7)), OMIM:146110)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000081311 - - - Unknown - - - - - Gemeinschaftspraxis für Humangenetik Dresden 00103196
0000279734 see paper; ..., primary amenorrhea, infertility, isolated deficiency pituitary FSH, normal LH primary amenorrhea, infertility HH24 Familial, autosomal recessive - - - - - Johan den Dunnen 00385933
0000279735 primary amenorrhea, isolated FSH deficiency primary amenorrhea HH24 Familial, autosomal recessive - - - - - Johan den Dunnen 00385934
0000279736 see paper; ..., delayed puberty, hypogonadism, FSH deficiency delayed puberty HH24 Familial, autosomal recessive - - - - - Johan den Dunnen 00385935
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