Phenotypes for disease #01974 (NPA (Niemann-Pick disease, type A (NPA)), OMIM:257200)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000254878 Lysosomal storage disease, developmental delay, conspicuous liver biopsy. Liver biopsy, cMRI abnormal (myelination disorder, dysplasia, grandfather with liver disease). - - Unknown 00y02m - - - - Andreas Laner 00359605
0000258185 HP:0002240 Hepatomegaly HP:0001744 Splenomegaly HP:0001263 Global developmental delay niemann-pick typeA niemann-pick typeA Familial, autosomal recessive - - - type A - Rezvan Abtahi 00362815
0000258198 HP:0002240 Hepatomegaly HP:0001744 Splenomegaly HP:0001263 Global developmental delay niemann-pick typeA niemann-pick typeA Familial, autosomal recessive - - - - - Rezvan Abtahi 00362828
0000258199 HP:0002240 Hepatomegaly HP:0001744 Splenomegaly HP:0002376 Developmental regression HP:0002540 Inability to walk niemann-pick typeA niemann-pick typeA Familial, autosomal recessive - - - type A - Rezvan Abtahi 00362829
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