Phenotypes for disease #04367 (PHPVAR (vitreous, primary, hyperplastic, persistent, autosomal recessive (PHPVAR)), OMIM:221900)

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

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000203111 persistent hyperplasia of the primary vitreous (PHPV, HP:0007968), gross nystagmus (HP:0000639) - congenital nonsyndromic persistent hyperplasia of the primary vitreous Familial, autosomal recessive - - - - - Jasmine Chen 00265313
Legend   How to query  


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