Phenotypes for disease #00132 (MDS (myelodysplastic syndrome (MDS)), OMIM:614286)

13 entries on 1 page. Showing entries 1 - 13.
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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000059850 - Unknown - - - - - Diagnosis: MDS - Gerard C.P. Schaafsma 00080286
0000059897 - Unknown - - - - - Diagnosis: Myelodysplastic syndrome - Gerard C.P. Schaafsma 00080333
0000059905 - Unknown - - - - - Diagnosis: MDS - Gerard C.P. Schaafsma 00080341
0000059932 - Unknown - - - - - Diagnosis: MDS - Gerard C.P. Schaafsma 00080368
0000059974 - Unknown - - - - - Diagnosis: MDS - Gerard C.P. Schaafsma 00080410
0000059987 - Unknown - - - - - Diagnosis: MDS - Gerard C.P. Schaafsma 00080423
0000060002 - Unknown - - - - - Diagnosis: MDS - Gerard C.P. Schaafsma 00080438
0000121438 Progressive Nonfluent Aphasia Familial, autosomal dominant 49y06m - - - - Language Impairment - Marc Cruts 00149020
0000121658 Progressive Nonfluent Aphasia Familial 72y - - - - - - Marc Cruts 00149240
0000121727 Progressive Nonfluent Aphasia Isolated (sporadic) - - - - - - - Marc Cruts 00149311
0000121787 Progressive Nonfluent Aphasia Unknown - - - - - - - Marc Cruts 00149371
0000121792 Progressive Nonfluent Aphasia Familial 53y - - - - - - Marc Cruts 00149376
0000121793 Progressive Nonfluent Aphasia Familial 53y - - - - - - Marc Cruts 00149377
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