Phenotypes for disease #02794 (HLD2;PMLD1 (leukodystrophy, hypomyelinating, type 2 (HLD-2, Pelizaeus-Merzbacher like disease 1 (PMLD-1))), OMIM:608804)

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000042023 Pelizaeus-Merzbacher like disease - - Familial - - - - - Michel van Geel 00055368
0000042024 Pelizaeus-Merzbacher like disease - - Familial - - - - - Michel van Geel 00055369
0000042025 Pelizaeus-Merzbacher like disease - - Familial - - - - - Michel van Geel 00055370
0000042026 Pelizaeus-Merzbacher like disease - - Isolated (sporadic) - - - - - Michel van Geel 00055371
0000042027 Pelizaeus-Merzbacher like disease - - Isolated (sporadic) - - - - - Michel van Geel 00055372
0000042028 Pelizaeus-Merzbacher like disease - - Unknown - - - - - Michel van Geel 00055373
0000042029 Pelizaeus-Merzbacher like disease - - Unknown - - - - - Michel van Geel 00055374
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