Phenotype #0000187833

Individual ID 00248866
Associated disease ?
Diagnosis/Initial craniofacial and cardiac syndrome
Diagnosis/Definite -
Phenotype details cleft lip/palate; no thin upper lip; no choanal atresia; ear anomaly; wide nasal bridge; broad nasal tip; no mid-facial hypoplasia; no mandibular prognathism; no brachycephaly; narrow, upslanted palpebral fissures; hooded eyelids; telecanthus; no high arched eyebrows; thin lateral eyebrows; no mild ectropion; no distichiasis; no ankyloblepahron; no ventricular septal defect; no tetralogy of Fallot; no atrial septal defect or patent foramen ovale; no no atrial septal defect or patent foramen ovale; no PS or coarctation aorta; no patent ductus arteriosus; no hypoplastic aortic arch; no autism spectrum disorder; no attention deficit hyperactivity disorder; developmental delay/learning difficulty; speech delay/language delay; aggressive behaviour; no anomalies hands; no anomalies feet; no voice anomalies; no skeletal anomalies; no short stature; no cancer;
Inheritance Familial, autosomal dominant
Age/Examination -
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 2019-07-29 19:36:23 +02:00 (CEST)
Date last edited 2019-08-02 17:05:45 +02:00 (CEST)

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