Phenotypes for disease #06379 (NEDCFSA (Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities), OMIM:618505)

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000290775 1y - Autism, Absent speech, Neurodevelopmental delay Unknown - - - - Andreas Laner 00397651
0000323964 - - Axial hypotonia, Strabismus, Neurodevelopmental delay, Hypotonia, Oral motor hypotonia, Epicanthus, Esodeviation, Hypomelanotic macule Isolated (sporadic) 01y - - - Andreas Laner 00433507
Legend   How to query  


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