STMN1, stathmin 1, 3925

N. diseases: 284; N. variants: 1
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.
Pancreatic Intraductal Papillary-Mucinous Adenoma
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 1 0.010 None 1.000 1 2017 2017
CUI: C4725675
Disease: Refractory Bladder Carcinoma
Refractory Bladder Carcinoma
disease Neoplastic Process 1 0.010 None 1.000 1 2011 2011
CUI: C0279603
Disease: Chondroblastic osteosarcoma
Chondroblastic osteosarcoma
disease Neoplastic Process 3 0.010 None 1.000 1 2018 2018
Stage IIA Esophageal Squamous Cell Carcinoma AJCC v7
disease Neoplastic Process 3 0.010 None 1.000 1 2014 2014
CUI: C0220775
Disease: RUSSELL-SILVER SYNDROME, X-LINKED
RUSSELL-SILVER SYNDROME, X-LINKED
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 4 0.010 None 1.000 1 2013 2013
CUI: C0232600
Disease: Self-induced vomiting
Self-induced vomiting
disease Pathological Conditions, Signs and Symptoms Mental or Behavioral Dysfunction 4 1 0.010 None 1.000 1 2011 2011
CUI: C1333172
Disease: Cutaneous Follicular Lymphoma
Cutaneous Follicular Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 5 0.010 None 1.000 1 2017 2017
Colorectal Intraepithelial Neoplasia
disease Digestive System Diseases; Neoplasms Neoplastic Process 6 0.010 None 1.000 1 2019 2019
CUI: C0270765
Disease: Myelopathic Muscular Atrophy
Myelopathic Muscular Atrophy
disease Nervous System Diseases Disease or Syndrome 7 0.010 None 1.000 1 1996 1996
CHROMOSOME Xq26.3 DUPLICATION SYNDROME
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 8 0.010 None 1.000 1 2014 2014
Endometrial neoplasm malignant metastatic
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 9 0.010 None 1.000 1 2014 2014
CUI: C0431122
Disease: Atypical meningioma
Atypical meningioma
disease Neoplasms; Nervous System Diseases Neoplastic Process 9 1 0.010 None 1.000 1 2017 2017
CUI: C1332184
Disease: Adult Atypical Meningioma
Adult Atypical Meningioma
disease Neoplastic Process 9 1 0.010 None 1.000 1 2017 2017
CUI: C4024957
Disease: Proximal spinal muscular atrophy
Proximal spinal muscular atrophy
disease Nervous System Diseases Disease or Syndrome 10 0.090 None 0.889 9 1995 2013
PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 11 1 0.010 None 1.000 1 2013 2013
CUI: C0205882
Disease: Infections, Parvovirus
Infections, Parvovirus
group Infections Disease or Syndrome 12 0.010 None 1.000 1 2002 2002
CUI: C0152109
Disease: Juvenile Spinal Muscular Atrophy
Juvenile Spinal Muscular Atrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 14 17 0.050 None 1.000 5 1996 2015
CUI: C1865384
Disease: Amyotrophy, monomelic
Amyotrophy, monomelic
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 15 2 0.010 None 1.000 1 2005 2005
CUI: C0037933
Disease: Spinal Diseases
Spinal Diseases
group Musculoskeletal Diseases Disease or Syndrome 16 0.030 None 1.000 3 2015 2017
CUI: C0017547
Disease: Gigantism
Gigantism
disease Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 16 1 0.020 None 1.000 2 2014 2015
CUI: C0917981
Disease: Progressive Muscular Atrophy
Progressive Muscular Atrophy
disease Nervous System Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 2013 2013
CUI: C0268274
Disease: Gangliosidoses, GM2
Gangliosidoses, GM2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 18 5 0.010 None 1.000 1 1997 1997
Heredodegenerative Disorders, Nervous System
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 18 0.010 None 1.000 1 2008 2008
CUI: C1511934
Disease: Differentiating Neuroblastoma
Differentiating Neuroblastoma
disease Neoplasms Neoplastic Process 20 0.010 None 1.000 1 2009 2009
CUI: C0008707
Disease: Chronic osteomyelitis
Chronic osteomyelitis
disease Infections; Musculoskeletal Diseases Disease or Syndrome 21 12 0.010 None 1.000 1 2017 2017