Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Platelet Storage Pool Deficiency
Hemic and Lymphatic Diseases
Hematologic Diseases
Hemorrhagic Disorders
Platelet Storage Pool Deficiency
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Platelet Disorders
Platelet Storage Pool Deficiency
Preferred term
Hermanski-Pudlak Syndrome
Type
-
Topical Descriptor
Broader concept
Entry terms
- Hermansky Pudlak Syndrome
- Hermansky-Pudlak Syndrome
Scope note
- Syndrome characterized by the triad of oculocutaneous albinism (ALBINISM, OCULOCUTANEOUS); PLATELET STORAGE POOL DEFICIENCY; and lysosomal accumulation of ceroid lipofuscin.
History note
- 2001
In other languages
-
Finnish
-
Hermanski-Pudlak
-
Hermanski-Pudlakin syndrooma
-
syndroma Hermanski-Pudlak
-
Swedish
URI
http://www.yso.fi/onto/mesh/D022861
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