National Library of Medicine - Medical Subject Headings

2013 MeSH

MeSH Descriptor Data

Return to Entry Page

Standard View. Go to Concept ViewGo to Expanded Concept View

Choroideremia
MeSH HeadingChoroideremia
Tree NumberC11.270.142
Tree NumberC11.941.160.300
Tree NumberC16.320.290.142
Tree NumberC16.320.322.092
Annotationof the eye, not of the choroid plexus: progressive degen in male, nonprogressive in female
Scope NoteAn X chromosome-linked abnormality characterized by atrophy of the choroid and degeneration of the retinal pigment epithelium causing night blindness.
Entry TermTapetochoroidal Dystrophy, Progressive
See AlsoNight Blindness
Allowable QualifiersBL CF CI CL CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
Previous Indexing Choroid (1966-1989)
Previous Indexing Eye Diseases (1966-1974)
Previous Indexing Uveal Diseases/genetics (1977-1989)
History Note90
Date of Entry19890525
Unique IDD015794


MeSH Tree Structures

 
Eye Diseases [C11]
   Eye Diseases, Hereditary [C11.270]
Aicardi Syndrome [C11.270.019]
Albinism [C11.270.040]  +
Aniridia [C11.270.060]  +
Arrow pointing to current tree nodeChoroideremia [C11.270.142]
Corneal Dystrophies, Hereditary [C11.270.162]  +
Duane Retraction Syndrome [C11.270.235]
Gyrate Atrophy [C11.270.468]
Leber Congenital Amaurosis [C11.270.516]
Optic Atrophies, Hereditary [C11.270.564]  +
Retinal Dysplasia [C11.270.660]
Retinitis Pigmentosa [C11.270.684]  +
Graves Ophthalmopathy [C11.270.842]
Walker-Warburg Syndrome [C11.270.881]
Weill-Marchesani Syndrome [C11.270.921]

 
Eye Diseases [C11]
   Uveal Diseases [C11.941]
      Choroid Diseases [C11.941.160]
Choroid Hemorrhage [C11.941.160.177]
Choroid Neoplasms [C11.941.160.238]
Choroidal Neovascularization [C11.941.160.244]
Arrow pointing to current tree nodeChoroideremia [C11.941.160.300]
Choroiditis [C11.941.160.478]  +
Gyrate Atrophy [C11.941.160.578]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
      Eye Diseases, Hereditary [C16.320.290]
Aicardi Syndrome [C16.320.290.019]
Albinism [C16.320.290.040]  +
Aniridia [C16.320.290.078]  +
Arrow pointing to current tree nodeChoroideremia [C16.320.290.142]
Corneal Dystrophies, Hereditary [C16.320.290.162]  +
Duane Retraction Syndrome [C16.320.290.235]
Gyrate Atrophy [C16.320.290.468]
Optic Atrophies, Hereditary [C16.320.290.564]  +
Retinal Dysplasia [C16.320.290.660]
Retinitis Pigmentosa [C16.320.290.684]  +
Vitelliform Macular Dystrophy [C16.320.290.763]
Weill-Marchesani Syndrome [C16.320.290.842]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
      Genetic Diseases, X-Linked [C16.320.322]
Aicardi Syndrome [C16.320.322.030]
Androgen-Insensitivity Syndrome [C16.320.322.061]
Barth Syndrome [C16.320.322.068]
Bulbo-Spinal Atrophy, X-Linked [C16.320.322.076]
Arrow pointing to current tree nodeChoroideremia [C16.320.322.092]
Dent Disease [C16.320.322.100]
Dyskeratosis Congenita [C16.320.322.108]
Ectodermal Dysplasia 1, Anhidrotic [C16.320.322.116]
Fabry Disease [C16.320.322.124]
Focal Dermal Hypoplasia [C16.320.322.186]
Glycogen Storage Disease Type IIb [C16.320.322.201]
Glycogen Storage Disease Type VIII [C16.320.322.217]
Granulomatous Disease, Chronic [C16.320.322.233]
Hemophilia B [C16.320.322.235]
Hyper-IgM Immunodeficiency Syndrome, Type 1 [C16.320.322.237]
Hypophosphatemic Rickets, X-Linked Dominant [C16.320.322.239]
Ichthyosis, X-Linked [C16.320.322.241]
Isolated Noncompaction of the Ventricular Myocardium [C16.320.322.370]
Mental Retardation, X-Linked [C16.320.322.500]  +
Muscular Dystrophy, Duchenne [C16.320.322.562]
Muscular Dystrophy, Emery-Dreifuss [C16.320.322.625]
Oculocerebrorenal Syndrome [C16.320.322.750]
Ornithine Carbamoyltransferase Deficiency Disease [C16.320.322.828]
Pelizaeus-Merzbacher Disease [C16.320.322.906]
Wiskott-Aldrich Syndrome [C16.320.322.937]
X-Linked Combined Immunodeficiency Diseases [C16.320.322.968]

Return to Entry Page Link to NLM Cataloging Classification