velocardiofacial
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VCF — velocardiofacial [syndrome]; velocity of circumferential fiber [lengthening]; ventricular contractility function … Medical dictionary
VCF syndrome — velocardiofacial syndrome a rare autosomal dominant syndrome of cardiac defects and characteristic craniofacial abnormalities including cleft palate, jaw abnormalities, and prominent nose. Learning disabilities occur often; short stature, slender … Medical dictionary
VCF — • velocardiofacial [syndrome]; • velocity of circumferential fiber [lengthening]; • ventricular contractility function … Dictionary of medical acronyms & abbreviations
22q11.2 deletion syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 3631 ICD10 = ICD10|D|82|1|d|80 ICD9 = ICD9|279.11, ICD9|758.32 ICDO = OMIM = 188400 MedlinePlus = eMedicineSubj = med eMedicineTopic = 567 eMedicine mult = eMedicine2|ped|589… … Wikipedia
CLDN5 — Claudin 5 (transmembrane protein deleted in velocardiofacial syndrome), also known as CLDN5, is a human gene.cite web | title = Entrez Gene: CLDN5 claudin 5 (transmembrane protein deleted in velocardiofacial syndrome)| url =… … Wikipedia
Hearing loss with craniofacial syndromes — is a common occurrence. Many of these multianomaly disorders involve structural malformations of the outer or middle ear, making a significant hearing loss highly likely. Treacher Collins syndrome Individuals with Treacher Collins syndrome often… … Wikipedia
ARVCF — Armadillo repeat gene deletes in velocardiofacial syndrome, also known as ARVCF, is a human gene.cite web | title = Entrez Gene: ARVCF armadillo repeat gene deletes in velocardiofacial syndrome| url =… … Wikipedia
DiGeorge syndrome — 22q11.2 deletion syndrome Classification and external resources Brain computer tomography cuts of t … Wikipedia
SEPT5 — Septin 5, also known as SEPT5, is a human gene.cite web | title = Entrez Gene: SEPT5 septin 5| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5413| accessdate = ] PBB Summary section title = summary text =… … Wikipedia
DGCR14 — DiGeorge syndrome critical region gene 14 Identifiers Symbols DGCR14; DGCR13; DGS H; DGS I; DGSH; DGSI; ES2; Es2el External IDs … Wikipedia
