Axenfeld anomaly syndrome
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Axenfeld anomaly — a developmental anomaly consisting of posterior embryotoxon and iris processes to the Schwalbe ring. Called also arcus juvenilis and posterior embryotoxon. See also anterior chamber cleavage syndrome, under syndrome … Medical dictionary
Axenfeld syndrome — Axenfeld anomaly accompanied by glaucoma and defective development of the corneoscleral trabecular meshwork and other angle structures. See also anterior chamber cleavage s … Medical dictionary
Axenfeld syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 30800 ICD10 = ICD9 = ICD9|743.44 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Axenfeld syndrome (also known as Axenfeld Rieger syndrome or Hagedoom syndrome) is the… … Wikipedia
anterior chamber cleavage syndrome — a term for several types of mesenchymal dysgenesis affecting neural crest derivatives in the iris, trabecula, and cornea. In ascending severity these disorders are: Axenfeld anomaly, Axenfeld syndrome, Rieger anomaly, and Rieger syndrome … Medical dictionary
Duane-radial ray syndrome — Classification and external resources OMIM 607323 DiseasesDB 33688 Duane radial ray syndrome is a rare disorder that affects the ey … Wikipedia
Tietz syndrome — Not to be confused with Tietze syndrome. Tietz syndrome Classification and external resources ICD 10 E70.3 (ILDS E70.358) OMIM 103500 … Wikipedia
Forkhead box C1 — Forkhead box C1, also known as FOXC1, is a human gene.cite web | title = Entrez Gene: FOXC1 forkhead box C1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=2296| accessdate = ] PBB Summary section title =… … Wikipedia
PITX2 — Paired like homeodomain transcription factor 2, also known as PITX2, is a human gene. PBB Summary section title = summary text = This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins.… … Wikipedia
Nonsyndromic deafness — is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Genetic changes are related to the following types of… … Wikipedia
Anterior segment mesenchymal dysgenesis — Classification and external resources OMIM 107250 Anterior segment dysgenesis (ASD) is a failure of the normal development of the tissues of the anterior segment of the eye. It leads to anomalies in the structure of the mature anterior segment,… … Wikipedia
