Phenotype #0000350361

Individual ID 00464307
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite SSMG
Phenotype details see paper; ..., birth 37w; intrauterine growth restriction; micrognathia; microcephaly; no cleft palate; tracheostomy; no congenital heart disease; no cataract; short stature; no rhizomelic shortening; joint laxity; no developmental delay/intellectual disability; no autism; no seizure; no carbohydrate deficient transferrin abnormalities; no giant cell hepatitis; normal liver function; no hepatoblastoma
Inheritance Isolated (sporadic)
Age/Examination 14y4m (14 years, 4 months)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
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 2025-03-01 09:13:49 +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.