Phenotype #0000187826

Individual ID 00248859
Associated disease ?
Diagnosis/Initial craniofacial and cardiac syndrome
Diagnosis/Definite -
Phenotype details cleft lip/palate; high-arched palate; no thin upper lip; no choanal atresia; ear anomaly; wide nasal bridge; broad nasal tip; mid-facial hypoplasia; mandibular prognathism; no brachycephaly; narrow, upslanted palpebral fissures; hooded eyelids; telecanthus; no high arched eyebrows; no thin lateral eyebrows; no mild ectropion; no distichiasis; no ankyloblepahron; hypodontia; no delayed dentition; 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; autism spectrum disorder; attention deficit hyperactivity disorder; developmental delay/learning difficulty; speech delay/language delay; aggressive behaviour; anomalies hands; anomalies feet; no voice anomalies; skeletal anomalies; no short stature; no cancer; velo-pharyngeal insufficiency, early onset puberty, bowel problems
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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