SYNONIMS: Progressive hemifacial atrophy
ICD10 code: L94.8
ORPHANET number: ORPHA1214
For more information about this disease, please visit the .
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Last modification: 10:47 28.08.2010
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SYNONIMS: Progressive hemifacial atrophy
ICD10 code: L94.8
ORPHANET number: ORPHA1214
For more information about this disease, please visit the .
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Last modification: 10:47 28.08.2010
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SYNONIMS: Hyperkeratosis Palmoplantaris with Periodontosis
Keratosis Palmoplantaris with Periodontopathia
Palmar-plantar Hyperkeratosis and Concomitant Periodontal Destruction
Palmoplantar Keratoderma with Periodontosis
ICD10 code: Q82.8
ORPHANET number: ORPHA678
For more information about this disease, please visit the Orphanet website.
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
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Last modification: 11:08 28.08.2010
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SYNONIMS: –
ICD10 code: J84.0
ORPHANET number: ORPHA60025
For more information about this disease, please visit the Orphanet website.
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
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Last modification: 10:47 21.05.2024
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SYNONIMS: Lobstein disease
ICD10 code: Q78.0
ORPHANET number: ORPHA666
For more information about this disease, please visit the Orphanet website.
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
RARE DISEASES LIBRARY:
You may find a detailed description of Osteogenesis Imperfecta in Issue 12 of “Rare Diseases & Orphan Drugs”. Click here to open the pdf-file (file size 690 KB).
You can subscribe for our free e-newsletter by entering your e-mail here.
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Last modification: 11:09 07.03.2013
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SYNONIMS: Barbeau Disease
ICD10 code: G71.0
ORPHANET number: ORPHA270
For more information about this disease, please visit the NIH Office of Rare Diseases Research website.
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Last modification: 11:10 28.08.2010
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SYNONIMS: Male Turner Syndrome
Female Pseudo-Turner Syndrome
Turner Phenotype With Normal Karyotype
ICD10 code: Q87.1
ORPHANET number: ORPHA648
For more information about this disease, please visit the Orphanet website.
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
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Last modification: 11:11 28.08.2010
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SYNONIMS: Sphingomyelinase deficiency
ICD10 code: E75.2
ORPHANET number: ORPHA645
For more information about this disease, please visit the Orphanet website.
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
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Last modification: 11:12 28.08.2010
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SYNONIMS: Von Recklinghausen disease
Peripheral neurofibromatosis
ICD10 code: Q85.0
ORPHANET number: ORPHA636
RESOURCES:
Patient registry of the Comprehensive NF Center at Washington University in St. Louis
Information for patients, prepared by the Comprehensive NF Center at Washington University in St. Louis
Information for medical professionals, prepared by the Comprehensive NF Center at Washington University in St. Louis
For more information about this disease, please visit the Orphanet website.
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
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Last modification: 10:13 05.03.2012
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SYNONIMS: –
ICD10 code: –
ORPHANET number: –
For more information about this disease, please visit the Orphanet website.
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
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Last modification: 11:14 27.08.2010
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SYNONIMS: Gelineau disease
ICD10 code: G47.4
ORPHANET number: ORPHA2073
For more information about this disease, please visit the Orphanet website.
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
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Last modification: 10:52 27.08.2010
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