NRAS, NRAS proto-oncogene, GTPase, 4893

N. diseases: 477; N. variants: 16
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: C1837732
Disease: Thickened helices
Thickened helices
phenotype Finding 23 0.100 0
Aplasia/Hypoplasia of the cerebellum
phenotype Finding 66 1 0.100 0
CUI: C1849089
Disease: Broad forehead
Broad forehead
phenotype Finding 95 2 0.100 0
CUI: C1849211
Disease: Generalized hirsutism
Generalized hirsutism
phenotype Finding 51 0.100 0
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness
phenotype Musculoskeletal Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms Sign or Symptom 338 30 0.100 0
CUI: C1849265
Disease: Overgrowth
Overgrowth
phenotype Finding 23 2 0.100 0
CUI: C0151669
Disease: Increased antibody level in blood
Increased antibody level in blood
phenotype Finding 11 0.100 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal
phenotype Finding 140 5 0.100 0
CUI: C0151311
Disease: Cranial nerve palsies
Cranial nerve palsies
phenotype Nervous System Diseases Disease or Syndrome 16 0.100 0
CUI: C0149978
Disease: Adenocarcinoma of rectum
Adenocarcinoma of rectum
disease Neoplastic Process 38 0.300 0
CUI: C1849677
Disease: Numerous nevi
Numerous nevi
phenotype Finding 5 0.100 0
CUI: C0085702
Disease: Monocytosis
Monocytosis
disease Disease or Syndrome 33 0.100 0
CUI: C1851731
Disease: Generalized overgrowth
Generalized overgrowth
phenotype Finding 23 0.100 0
CUI: C1848490
Disease: Protruding eyes
Protruding eyes
phenotype Finding 136 0.100 0
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation
group Finding 38 0.100 0
CUI: C1837760
Disease: Prominent eyes
Prominent eyes
phenotype Finding 136 0.100 0
CUI: C1837761
Disease: Narrow nasal ridge
Narrow nasal ridge
phenotype Finding 7 0.100 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency
disease Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms Mental or Behavioral Dysfunction 1031 0.100 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion
phenotype Finding 77 0.100 0
CUI: C1839797
Disease: Deep philtrum
Deep philtrum
phenotype Finding 28 1 0.100 0
CUI: C0206620
Disease: Lymphangioma, Cystic
Lymphangioma, Cystic
disease Neoplasms Neoplastic Process 28 0.100 0
CUI: C1842820
Disease: Cardiac conduction abnormality
Cardiac conduction abnormality
phenotype Finding 101 0.100 0
CUI: C1843367
Disease: Poor school performance
Poor school performance
phenotype Finding 984 116 0.100 0
CUI: C0162835
Disease: Hypopigmentation disorder
Hypopigmentation disorder
group Skin and Connective Tissue Diseases Disease or Syndrome 72 5 0.100 0
CUI: C0158995
Disease: Congenital anemia
Congenital anemia
disease Disease or Syndrome 208 0.300 limited 0