Phenotypes for disease #00651 (HH2;KAL2 (hypogonadism, hypogonadotropic, type 2 with/without anosmia (HH2)), OMIM:147950)

5 entries on 1 page. Showing entries 1 - 5.
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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     
0000061013 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00037765
0000073457 Split hand foot malformation Hypogonadotripic hypogonadism - - Isolated (sporadic) 17y - - - - Kohnosuke Ohtaka 00095072
0000073458 Split hand hoot malformation Hypogonadtropic hypogonadism - - Unknown 34y - - - - Kohnosuke Ohtaka 00095073
0000073459 Split hand foot malformation Hypogonadotropic hypogonadism - - Familial, autosomal dominant 00y - - - - Kohnosuke Ohtaka 00095074
0000073473 - - - Unknown - - - - - Kohnosuke Ohtaka 00094957
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