Phenotypes for disease #01994 (OPTB3 (osteopetrosis, autosomal recessive, type 3), OMIM:259730)

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     
0000060440 Osteopetrosis, autosomal recessive 3, with renal tubular acidosis (OMIM:259730) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080871
0000060487 Osteopetrosis, autosomal recessive 3, with renal tubular acidosis (OMIM:259730) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080918
0000324508 osteopetrosis, renal tubular acidosis, cerebral calcification, blindness, deafness, development delay, amelogenesis imperfecta - - Familial, autosomal recessive - - - - - Juliana Mazzeu 00434153
Legend   How to query  


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