Phenotypes for disease #05108 (ECTDO (dysplasia, ectodermal, with oligodontia (ECTDO)))

4 entries on 1 page. Showing entries 1 - 4.
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     
0000043036 ectodermal dysplasia (HP:0000968), oligodontia (HP:0000677) - - Familial, autosomal recessive - - - - - Mary-Claire King 00056411
0000043037 ectodermal dysplasia (HP:0000968), oligodontia (HP:0000677) - - Familial, autosomal recessive - - - - - Mary-Claire King 00056428
0000043038 ectodermal dysplasia (HP:0000968), oligodontia (HP:0000677) - - Familial, autosomal recessive - - - - - Mary-Claire King 00056429
0000043039 ectodermal dysplasia (HP:0000968), oligodontia (HP:0000677) - - Familial, autosomal recessive - - - - - Mary-Claire King 00056430
Legend   How to query  


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