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SYNONIMS: Hashimoto struma
Hashimoto hypothyroidism

ICD10 code: E06.3

ORPHANET number: ORPHA855

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: 10:04 27.08.2010
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SYNONIMS: Chronic benign familial pemphigus

ICD10 code: Q82.8

ORPHANET number: ORPHA2841

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: 07:15 29.08.2010
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DISEASE NAME: Hereditary angioedema (HAE)

SYNONIMS: Familial angioneurotic edema, HAE, Hereditary angioneurotic edema, Hereditary bradykinine-induced angioedema, Hereditary non histamine-induced angioedema

ICD10 code: D84.1

ORPHANET number: ORPHA91378

For more information about this disease, please visit the

SYNONIMS: Oculo-auriculo-vertebral anomaly
Goldenhar-Gorlin syndrome
Hemifacial microsomia

ICD10 code: Q87.0

ORPHANET number: ORPHA374

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: 07:12 29.08.2010
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SYNONIMS: Gilles de la Tourette syndrome

ICD10 code: F95.2

ORPHANET number: ORPHA856

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: 07:20 29.08.2010
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Sorry, this entry is only available in Bulgarian.

SYNONIMS: Primary chronic sclerosing osteomyelitis
Proliferative periostitis
Sclerosing periostitis

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: 06:52 29.08.2010
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