| Descriptor English: | Stargardt Disease | ||||||
| Descriptor Spanish: |
Enfermedad de Stargardt
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| Descriptor Portuguese: | Doença de Stargardt | ||||||
| Descriptor French: | Maladie de Stargardt | ||||||
| Entry term(s): |
Degeneration, Juvenile Macular Degeneration, Stargardt Macular Fundus Flavimaculatus Juvenile Macular Degeneration Juvenile Macular Degenerations Macular Degeneration, Juvenile Macular Degeneration, Stargardt Macular Dystrophy With Flecks, Type 1 Stargardt Disease 1 Stargardt Macular Degeneration Stargardt Macular Degenerations |
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| Tree number(s): |
C11.270.872 C11.768.585.439.339 C16.320.290.724 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000080362 | ||||||
| Scope note: | A juvenile-onset macular dystrophy characterized by progressive loss of VISUAL ACUITY with normal acuity in peripheral VISUAL FIELDS. Other associated clinical features may include LIPOFUSCIN fundus autofluorescence, atrophy of the RETINAL PIGMENT EPITHELIUM, loss of color vision, PHOTOPHOBIA and PARACENTRAL SCOTOMA. Germline mutations in the ABCA4 gene have been identified in recessive and dominant diseases. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 2020; STARGARDT DISEASE was indexed under MACULAR DEGENERATION 2010-2019 |
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| History Note: | 2020(2010) |
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| DeCS ID: | 59247 | ||||||
| Unique ID: | D000080362 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2020/01/01 | ||||||
| Date of Entry: | 2019/07/08 | ||||||
| Revision Date: | 2019/04/29 |
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DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases
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Stargardt Disease
- Preferred
Stargardt Disease 1
- Narrower
Juvenile Macular Degeneration
- Narrower
| Concept UI |
M000612272 |
| Scope note | A juvenile-onset macular dystrophy characterized by progressive loss of VISUAL ACUITY with normal acuity in peripheral VISUAL FIELDS. Other associated clinical features may include LIPOFUSCIN fundus autofluorescence, atrophy of the RETINAL PIGMENT EPITHELIUM, loss of color vision, PHOTOPHOBIA and PARACENTRAL SCOTOMA. Germline mutations in the ABCA4 gene have been identified in recessive and dominant diseases. |
| Preferred term | Stargardt Disease |
| Entry term(s) |
Degeneration, Stargardt Macular Fundus Flavimaculatus Macular Degeneration, Stargardt Stargardt Macular Degeneration Stargardt Macular Degenerations |
| Concept UI |
M0530265 |
| Preferred term | Stargardt Disease 1 |
| Entry term(s) |
Macular Dystrophy With Flecks, Type 1 |
| Concept UI |
M000612276 |
| Preferred term | Juvenile Macular Degeneration |
| Entry term(s) |
Degeneration, Juvenile Macular Juvenile Macular Degenerations Macular Degeneration, Juvenile |
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