Phenotypes for disease #02924 (DFNB67 (deafness, autosomal recessive, type 67 (DFNB-67)), OMIM:610265)

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     
0000124364 bilateral profound deafness, walking delay, bilateral vestibular areflexia Usher syndrome DFNB-67 Familial, autosomal recessive 01y 01y06m 00y 0y - Justine Lerat 00152005
0000337684 - Hearing loss - Unknown - - - - - Hina Khan 00448501
Legend   How to query  


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