Summative Diagnosis:
Cardiovascular Phenotype: Persistent truncus arteriosis (PTA, Type A1, A2, A4), permembranous ventricular septal defects (pmVSD) and muscular ventricular septal defect (mVSD), right aortic arch (RAA), ventricular non-compaction, ventricular hypertrophy
Noncardiovascular Phenotype: Short snout, anophthalmia/microphthalmia, short snount/micrognathia, hypoplastic thymus, incomplete closure of the umbilical herniation, cystic kidneys, hydrnephrosis, hooked tail

Fyler Codes
The Fyler code developed by The Boston Children's Heart Foundation in Boston Children's Hospital provides a hierarchical clinical diagnosis of congenital cardiovascular defects and other disorders. These codes are used to delineate pathology in the mutant mouse models that parallel human disease and can be cross referenced to the International Pediatric and Congenital Cardiac Code (IPCCC) (http://www.ipccc.net/).

Fyler Code ID	Code Description
0500	Truncus arteriosus
1300	Ventricular septal defect
1310	Ventricular septal defect, membranous
1320	Ventricular septal defect, muscular
1802	Excessive myocardial trabeculation or noncompaction
2700	Abnormal aortic arch
2720	Right aortic arch
4163	Micrognathia
4502	Hydronephrosis
4864	Anophthalmia
4877	Microphthalmia
4906	Non-cardiac abnormality
4907	Non-cardiac thoracic abnormality
7505	Biventricular hypertrophy