| Descriptor English: | Pseudoxanthoma Elasticum | ||||||
| Descriptor Spanish: |
Seudoxantoma Elástico
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| Descriptor Portuguese: | Pseudoxantoma Elástico | ||||||
| Descriptor French: | Pseudoxanthome élastique | ||||||
| Entry term(s): |
Elasticum, Incomplete Pseudoxanthoma Elasticums, Incomplete Pseudoxanthoma Groenblad-Strandberg Syndrome Gronblad Strandberg Syndrome Gronblad-Strandberg Syndrome Incomplete Pseudoxanthoma Elasticum Incomplete Pseudoxanthoma Elasticums Pseudoxanthoma Elasticum, Autosomal Dominant Pseudoxanthoma Elasticum, Forme Fruste Pseudoxanthoma Elasticum, Incomplete Pseudoxanthoma Elasticums, Incomplete Syndrome, Gronblad-Strandberg |
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| Tree number(s): |
C14.907.454.530 C15.378.463.515.530 C16.131.831.766 C16.320.850.750 C17.300.766 C17.800.804.766 C17.800.827.750 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D011561 | ||||||
| Scope note: | An inherited disorder of connective tissue with extensive degeneration and calcification of ELASTIC TISSUE primarily in the skin, eye, and vasculature. At least two forms exist, autosomal recessive and autosomal dominant. This disorder is caused by mutations of one of the ATP-BINDING CASSETTE TRANSPORTERS. Patients are predisposed to MYOCARDIAL INFARCTION and GASTROINTESTINAL HEMORRHAGE. |
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| Annotation: | in titles & translations use diacritic: Grönblad |
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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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| DeCS ID: | 11998 | ||||||
| Unique ID: | D011561 | ||||||
| NLM Classification: | WD 375 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1966/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2015/06/18 |
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Pseudoxanthoma Elasticum
- Preferred
Gronblad-Strandberg Syndrome
- Narrower
Pseudoxanthoma Elasticum, Incomplete
- Narrower
| Concept UI |
M0017968 |
| Scope note | An inherited disorder of connective tissue with extensive degeneration and calcification of ELASTIC TISSUE primarily in the skin, eye, and vasculature. At least two forms exist, autosomal recessive and autosomal dominant. This disorder is caused by mutations of one of the ATP-BINDING CASSETTE TRANSPORTERS. Patients are predisposed to MYOCARDIAL INFARCTION and GASTROINTESTINAL HEMORRHAGE. |
| Preferred term | Pseudoxanthoma Elasticum |
| Concept UI |
M0017969 |
| Preferred term | Gronblad-Strandberg Syndrome |
| Entry term(s) |
Groenblad-Strandberg Syndrome Gronblad Strandberg Syndrome Syndrome, Gronblad-Strandberg |
| Concept UI |
M0501068 |
| Preferred term | Pseudoxanthoma Elasticum, Incomplete |
| Entry term(s) |
Elasticum, Incomplete Pseudoxanthoma Elasticums, Incomplete Pseudoxanthoma Incomplete Pseudoxanthoma Elasticum Incomplete Pseudoxanthoma Elasticums Pseudoxanthoma Elasticum, Autosomal Dominant Pseudoxanthoma Elasticum, Forme Fruste Pseudoxanthoma Elasticums, Incomplete |
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