Phenotypes for disease #01702 (PBD1A (peroxisome biogenesis disorder, type 1A (PBD1A, Zellweger syndrome)), OMIM:214100)

3 entries on 1 page. Showing entries 1 - 3.
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     
0000060588 Peroxisome biogenesis disorder 1A (Zellweger) (OMIM:214100) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081019
0000231984 - - - Familial, autosomal recessive - - - - - Sha Hong 00306140
0000301676 best corrected visual acuity: 1.2; electroretinogram , rod: n.a., cone: n.a. - dystrophy, corneoretinal, crystalline, Bietti (BCD) Familial, autosomal recessive 36y - 35y - - LOVD 00409559
Legend   How to query  


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