Phenotypes for disease #01484 (osteoporosis, OMIM:166710)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000254091 Idiopathic osteoporosis Idiopathic osteoporosis - Familial - - - - - Frans Cremers 00107694
0000254092 Idiopathic osteoporosis Idiopathic osteoporosis - Familial - - - - - Frans Cremers 00107695
0000254093 primary osteoporosis primary osteoporosis - Familial - - - - - Frans Cremers 00107704
0000254094 idiopathic osteoporosis idiopathic osteoporosis - Familial - - - - - Frans Cremers 00107706
0000254095 primary osteoporosis primary osteoporosis - Familial - - - - - Frans Cremers 00107711
0000292653 Bone pain (HP:0002653), Myopia (HP:0000545), Polycystic Ovary Syndrome 1 (OMIM:184700), Bipolar affective disorder (HP:0007302), Psoriasiform dermatitis (HP:0003765), Long foot (HP:0001833), Mandibular prognathia (HP:0000303) osteoporosis osteoporosis Familial, autosomal dominant 33y 33y - - - Litika Vermani 00398661
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