Phenotype #0000187829

Individual ID 00248862
Associated disease ?
Diagnosis/Initial craniofacial and cardiac syndrome
Diagnosis/Definite -
Phenotype details cleft lip/palate; no high-arched palate; no thin upper lip; no choanal atresia; ear anomaly; wide nasal bridge; no broad nasal tip; mid-facial hypoplasia; no mandibular prognathism; no brachycephaly; no narrow, upslanted palpebral fissures; no hooded eyelids; no telecanthus; high arched eyebrows; thin lateral eyebrows; mild ectropion; no distichiasis; no ankyloblepahron; no hypodontia; no delayed dentition; no abnormal crown form; 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; no developmental delay/no learning difficulty; no speech delay/no language delay; no aggressive behaviour; anomalies hands; anomalies feet; voice anomalies; skeletal anomalies, scoliosis; short stature; no cancer; hypothyroid
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)

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