Phenotypes for disease #05516 (HPANBH4 (hyperphenylalaninemia, mild, non-BH4-deficient (HPANBH4)), OMIM:617384)

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000154686 hyperphenylalaninemia HPANBH4 hyperphenylalaninemia (HP:0004923) Familial, autosomal recessive - - - - - Belen Perez 00180961
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.