Phenotypes for disease #06629 (GINGF5 (fibromatosis, gingival, type 5), OMIM:617626)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000311282 gingival fibromatosis and hearing loss Jones syndrome - Familial, autosomal dominant - - - - Elisa Rahikkala 00416320
0000311283 gingival fibromatosis and hearing loss Jones syndrome - Familial, autosomal dominant - - - - Elisa Rahikkala 00420046
0000311285 gingival fibromatosis and hearing loss Jones syndrome - Familial, autosomal dominant - - - - Elisa Rahikkala 00420048
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