Phenotypes for disease #03526 (Emberger syndrome, OMIM:614038)

8 entries on 1 page. Showing entries 1 - 8.
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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     
0000185677 Primary lymphoedema associated with a predisposition to acute myeloid leukemia - - Familial, autosomal dominant - - - - - LOVD 00245831
0000185678 Primary lymphoedema associated with a predisposition to acute myeloid leukemia - - Familial, autosomal dominant - - - - - LOVD 00245832
0000185680 Primary lymphoedema associated with a predisposition to acute myeloid leukemia - - Unknown - - - - - LOVD 00245835
0000185681 Primary lymphoedema associated with a predisposition to acute myeloid leukemia / Sporadic? (parents not tested) - - Isolated (sporadic) - - - - - LOVD 00245836
0000185682 Primary lymphoedema associated with a predisposition to acute myeloid leukemia / Sporadic? (parents not tested) - - Isolated (sporadic) - - - - - LOVD 00245837
0000185683 Primary lymphoedema associated with a predisposition to acute myeloid leukemia / Sporadic? (parents not tested) - - Isolated (sporadic) - - - - - LOVD 00245838
0000185684 Primary lymphoedema associated with a predisposition to acute myeloid leukemia - - Unknown - - - - - LOVD 00245839
0000185685 Primary lymphoedema associated with a predisposition to acute myeloid leukemia / Sporadic? (parents not tested) - - Isolated (sporadic) - - - - - Pia Ostergaard 00245840
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