Phenotype #0000168016

Individual ID 00222896
Associated disease ID
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Phenotype details see paper; ..., developmental delay, full-scale IQ 52, deep-set eyes, infra-orbital creases, malar flattening, upturned nares,, wide cupid-bow mouth, full lips, low setears posteriorly rotated, mild 5th finger clinodactyly and mild camptodactyly
Age/Examination 08y10m (8 years, 10 months)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-02-12 21:51:10 +01:00 (CET)
Date last edited N/A

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