Phenotype #0000187825

Individual ID 00248858
Associated disease ?
Diagnosis/Initial craniofacial and cardiac syndrome
Diagnosis/Definite -
Phenotype details no cleft lip/palate; high-arched palate; thin upper lip; choanal atresia; ear anomaly; wide nasal bridge; no broad nasal tip; mid-facial hypoplasia; no mandibular prognathism; brachycephaly; no narrow, upslanted palpebral fissures; no hooded eyelids; no telecanthus; high arched eyebrows; no thin lateral eyebrows; no mild ectropion; distichiasis; ankyloblepahron; hypodontia; delayed dentition; abnormal crown form; ventricular septal defect; no tetralogy of Fallot; atrial septal defect or patent foramen ovale; no no atrial septal defect or patent foramen ovale; no PS or coarctation aorta; patent ductus arteriosus; no hypoplastic aortic arch;; attention deficit hyperactivity disorder; developmental delay/learning difficulty; no speech delay/no language delay; aggressive behaviour; no anomalies hands; anomalies feet; voice anomalies; no skeletal anomalies; no short stature; no cancer; partial agenesis corpus callosum
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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