PDCD10, programmed cell death 10, 11235

N. diseases: 68; N. variants: 11
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0025286
Disease: Meningioma
Meningioma
disease Neoplasms; Nervous System Diseases Neoplastic Process 634 43 0.100 None 0
CUI: C0027858
Disease: Neuroma
Neuroma
disease Neoplasms Neoplastic Process 15 0.100 None 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
disease Musculoskeletal Diseases Disease or Syndrome 850 135 0.100 None 0
Focal T2 hyperintense brainstem lesion
phenotype Finding 33 2 0.100 None 0
CUI: C0151740
Disease: Intracranial Hypertension
Intracranial Hypertension
disease Nervous System Diseases Finding 72 1 0.100 None 0
Arteriovenous Malformations, Cerebral
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Congenital Abnormality 35 6 0.100 None 0 1
CUI: C0162819
Disease: Skin Diseases, Vascular
Skin Diseases, Vascular
group Skin and Connective Tissue Diseases Disease or Syndrome 11 2 0.100 None 0
CUI: C0730304
Disease: Cavernous hemangioma of retina
Cavernous hemangioma of retina
disease Neoplasms; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 3 0.100 None 0
CUI: C0241224
Disease: Spinal cord lesion
Spinal cord lesion
phenotype Nervous System Diseases Finding 7 0.100 None 0
CUI: C0265950
Disease: Venous malformation
Venous malformation
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 38 3 0.100 None 0
CUI: C0544886
Disease: Somatic mutation
Somatic mutation
phenotype Cell or Molecular Dysfunction 151 0.100 None 0
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
disease Mental Disorders Mental or Behavioral Dysfunction 1630 348 0.100 None 0
CUI: C0346390
Disease: Hemangioma of choroid
Hemangioma of choroid
disease Neoplasms; Cardiovascular Diseases Neoplastic Process 4 2 0.100 None 0
CUI: C0522224
Disease: Paralysed
Paralysed
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 68 0.100 None 0
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting
phenotype Pathological Conditions, Signs and Symptoms Finding 43 10 0.100 None 0
Other malformations of cerebral vessels
disease Congenital Abnormality 2 0.200 None 0
Focal T2 hypointense brainstem lesion
phenotype Finding 3 0.100 None 0
CUI: C4021762
Disease: Abnormality of the cerebrum
Abnormality of the cerebrum
disease Anatomical Abnormality 4 0.100 None 0
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 122 78 0.100 None 0
CUI: C2937220
Disease: Congenital abnormality of vein
Congenital abnormality of vein
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 39 7 0.100 None 0
Nonruptured congenital cerebral aneurysm
disease Disease or Syndrome; Congenital Abnormality 2 0.200 None 0
Congenital malformation of cerebral vessels NOS
disease Congenital Abnormality 2 0.200 None 0
CUI: C1956261
Disease: Cerebral Venous Angioma
Cerebral Venous Angioma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases; Cardiovascular Diseases Congenital Abnormality 4 0.200 None 0
CUI: C0018681
Disease: Headache
Headache
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 338 75 0.100 None 0
CUI: C0018989
Disease: Hemiparesis
Hemiparesis
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 91 6 0.100 None 0 1