MeSH Treeview
Query OMIM entry list
139090
GPS
GRAY PLATELET SYNDROME
→
High-scoring List
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Marfan Syndrome
Joint Diseases
Hemarthrosis
Stomatognathic Diseases
Mouth Diseases
Oral Hemorrhage
Eye Diseases
Eye Diseases, Hereditary
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Heart Diseases
Heart Defects, Congenital
Marfan Syndrome
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Bernard-Soulier Syndrome
Hemophilia A
Hermanski-Pudlak Syndrome
Thrombasthenia
von Willebrand Diseases
Wiskott-Aldrich Syndrome
Coagulation Protein Disorders
Hemophilia A
von Willebrand Diseases
Platelet Storage Pool Deficiency
Hermanski-Pudlak Syndrome
Purpura
Purpura, Thrombocytopenic
Purpura, Thrombocytopenic, Idiopathic
Blood Platelet Disorders
Bernard-Soulier Syndrome
Platelet Storage Pool Deficiency
Hermanski-Pudlak Syndrome
Thrombasthenia
Thrombocytopenia
Thrombotic Microangiopathies
Purpura, Thrombocytopenic
Purpura, Thrombocytopenic, Idiopathic
von Willebrand Diseases
Hemorrhagic Disorders
Bernard-Soulier Syndrome
Hemophilia A
Platelet Storage Pool Deficiency
Hermanski-Pudlak Syndrome
Purpura, Thrombocytopenic, Idiopathic
Thrombasthenia
von Willebrand Diseases
Wiskott-Aldrich Syndrome
Leukocyte Disorders
Leukopenia
Lymphopenia
Wiskott-Aldrich Syndrome
Phagocyte Bactericidal Dysfunction
Chediak-Higashi Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Marfan Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Bernard-Soulier Syndrome
Hemophilia A
Hermanski-Pudlak Syndrome
Thrombasthenia
von Willebrand Diseases
Wiskott-Aldrich Syndrome
Eye Diseases, Hereditary
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Genetic Diseases, X-Linked
Wiskott-Aldrich Syndrome
Marfan Syndrome
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin Diseases, Genetic
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Marfan Syndrome
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Skin Diseases, Genetic
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Oculocutaneous
Hermanski-Pudlak Syndrome
Immune System Diseases
Autoimmune Diseases
Purpura, Thrombocytopenic, Idiopathic
Immunologic Deficiency Syndromes
Lymphopenia
Wiskott-Aldrich Syndrome
Phagocyte Bactericidal Dysfunction
Chediak-Higashi Syndrome
Wiskott-Aldrich Syndrome
Purpura, Thrombocytopenic
Purpura, Thrombocytopenic, Idiopathic
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Splenomegaly
Pathologic Processes
Disease
Syndrome
Disease Attributes
Diseases in Twins
Hemorrhage
Hemarthrosis
Oral Hemorrhage
Purpura
Purpura, Thrombocytopenic
Purpura, Thrombocytopenic, Idiopathic
Signs and Symptoms
Oral Manifestations
Oral Hemorrhage
Skin Manifestations
Purpura
Purpura, Thrombocytopenic
Purpura, Thrombocytopenic, Idiopathic
Database Center for Life Science
