Phenotypes for disease #03766 (PBD7B (peroxisome biogenesis disorder, type 7B (PBD-7B)), OMIM:614873)

2 entries on 1 page. Showing entries 1 - 2.
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     
0000300900 sensorineural hearing impairment (HP:0000407); bilateral, prelingual onset, moderate-profound, apparently non progressive; ataxia (HP:0001251), onset 2y, stable/slowly progressive; yellow-brown teeth by probable amelogenesis imperfecta (HP:0006286 ), permanent teeth yellow-brown and worn, had several cavities, lost several dental pieces; ,40y cessation of menses (HP:0008209); pubertal development, 13y-menarche Zelweger Spectrum Disorder (Heimler Syndrome)/Perraul Syndrome. PBD7B Familial, autosomal recessive 47y 49y 02y - - Guillermina García Sánchez 00408755
0000300910 sensorineural hearing impairment (HP:0000407), bilateral, prelingual onset, profound; ataxia (HP:0001251) onset2y, stable/slowly progressive; yellow-brown teeth by probable amelogenesis imperfecta (HP:0006286), permanent teeth yellow-brown and worn, several cavities, lost several dental pieces; <40y-cessation of menses (HP:0008209); 13y- menarche Zelweger Spectrum Disorder (Heimler Syndrome)/Perraul Syndrome PDB7B Familial, autosomal recessive 45y 47y 02y - - Guillermina García Sánchez 00408756
Legend   How to query  


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