Phenotypes for disease #04095 (XIGIS;MRD25 (Xia-Xibbs syndrome (XIGIS, MRD25)), OMIM:615829)

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     
0000171203 global developmental delay (HP:0001263), hypoplasia corpus callosum (HP:0002079), laryngomalacia (HP:0001601), lack of speech (HP:0001344) Xia-Gibbs syndrome MRD-25 Isolated (sporadic) 01y 02y 02y - - Evren Gumus 00226093
0000174748 convulsion, neurovelopmental disease, sleep apnea - Xia-Gibbs syndrome Isolated (sporadic) 08y 14y - - AHDC1 Augusto César Cardoso-dos-Santos 00234329
0000300937 Bilateral tonic-clonic seizure, Generalized non-motor (absence) seizure, Global developmental delay, Neurodevelopmental delay - - Isolated (sporadic) 16y - - - - Andreas Laner 00408818
Legend   How to query  


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