MeSH Treeview
Query OMIM entry list
601273
CLTCL1
CLATHRIN, HEAVY POLYPEPTIDE-LIKE 1
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Nerve Tissue
Meningioma
Neoplasms, Vascular Tissue
Meningioma
Neoplasms by Site
Nervous System Neoplasms
Central Nervous System Neoplasms
Meningeal Neoplasms
Meningioma
Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Nervous System Diseases
Nervous System Neoplasms
Central Nervous System Neoplasms
Meningeal Neoplasms
Meningioma
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
22q11 Deletion Syndrome
DiGeorge Syndrome
Heart Diseases
Heart Defects, Congenital
22q11 Deletion Syndrome
DiGeorge Syndrome
Hemic and Lymphatic Diseases
Lymphatic Diseases
Lymphatic Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
22q11 Deletion Syndrome
DiGeorge Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
22q11 Deletion Syndrome
DiGeorge Syndrome
Chromosome Disorders
22q11 Deletion Syndrome
DiGeorge Syndrome
Lymphatic Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Musculoskeletal Abnormalities
Craniofacial Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
22q11 Deletion Syndrome
DiGeorge Syndrome
Endocrine System Diseases
Parathyroid Diseases
Hypoparathyroidism
22q11 Deletion Syndrome
DiGeorge Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Translocation, Genetic
Disease
Syndrome
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