Phenotypes for disease #00275 (MOPD2 (dwarfism, primordial, osteodysplastic, microcephalic type II), OMIM:210720)

9 entries on 1 page. Showing entries 1 - 9.
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     
0000060520 Microcephalic osteodysplastic primordial dwarfism, type II (OMIM:210720) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080951
0000090172 Mild intellectual disability - - Unknown - - - - - Emmelien Aten 00114690
0000090173 Mild intellectual disability - - Unknown - - - - - Emmelien Aten 00114691
0000090175 - - - Unknown - - - - - Emmelien Aten 00114693
0000090177 - - - Unknown - - - - - Emmelien Aten 00114695
0000090180 - - - Unknown - - - - - Emmelien Aten 00114698
0000090182 Severe intellectual disability - - Unknown - - - - - Emmelien Aten 00114700
0000090183 - - - Unknown - - - - - Emmelien Aten 00114701
0000090184 - - - Unknown - - - - - Emmelien Aten 00114702
Legend   How to query  


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