Phenotypes for disease #00452 (PSAPD (saposin deficiency, combined (PSAPD)), OMIM:611721)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000016225 HPLC analysis of normal and saposin B-deficient lymphoblasts showed no saposin A, C, or D deficiency - - Isolated (sporadic) - - - - - Johan den Dunnen 00017866
0000060464 Combined SAP deficiency (OMIM:611721) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080895
0000060489 Combined SAP deficiency (OMIM:611721) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080920
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