CALM3, calmodulin 3, 808

N. diseases: 215; N. variants: 3
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: C3826614
Disease: Cardiac arrest in children
Cardiac arrest in children 		disease Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2016 2016
CUI: C1708957
Disease: Mediastinal Paraganglioma
Mediastinal Paraganglioma 		disease Neoplastic Process 5 2 0.010 None 1.000 1 2019 2019
CUI: C1833372
Disease: HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III 		disease Nutritional and Metabolic Diseases Disease or Syndrome 5 2 0.010 None 1.000 1 1999 1999
CUI: C3203503
Disease: Mixed delirium
Mixed delirium 		disease Mental or Behavioral Dysfunction 5 0.010 None 1.000 1 2017 2017
CUI: C0339084
Disease: Floppy lid syndrome
Floppy lid syndrome 		disease Eye Diseases Disease or Syndrome 6 0.010 None 1.000 1 2010 2010
CUI: C0432593
Disease: Varus angulation
Varus angulation 		disease Musculoskeletal Diseases Anatomical Abnormality 6 0.010 None 1.000 1 2017 2017
CUI: C4524517
Disease: cutaneous squamous cell carcinoma of the head and neck
cutaneous squamous cell carcinoma of the head and neck 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 6 0.010 None 1.000 1 2009 2009
CUI: C0678255
Disease: polydrug use
polydrug use 		disease Mental or Behavioral Dysfunction 7 0.010 None 1.000 1 2020 2020
CUI: C3203501
Disease: Hypoactive delirium
Hypoactive delirium 		disease Mental or Behavioral Dysfunction 7 0.010 None 1.000 1 2017 2017
CUI: C1334411
Disease: Locally Metastatic Malignant Neoplasm
Locally Metastatic Malignant Neoplasm 		disease Neoplastic Process 8 0.010 None 1.000 1 2019 2019
CUI: C1855263
Disease: Disorganized thinking
Disorganized thinking 		disease Mental or Behavioral Dysfunction 8 0.010 None 1.000 1 2018 2018
CUI: C1837610
Disease: ICHTHYOSIS PREMATURITY SYNDROME
ICHTHYOSIS PREMATURITY SYNDROME 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 9 6 0.010 None 1.000 1 2018 2018
CUI: C3164344
Disease: Adult onset autosomal dominant leukodystrophy
Adult onset autosomal dominant leukodystrophy 		disease Disease or Syndrome 9 0.010 None 1.000 1 2010 2010
CUI: C1969623
Disease: NEUROFIBROMATOSIS, TYPE 1-LIKE SYNDROME
NEUROFIBROMATOSIS, TYPE 1-LIKE SYNDROME 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 13 32 0.010 None 1.000 1 2017 2017
CUI: C0268147
Disease: Glycogen storage disease, type IX
Glycogen storage disease, type IX 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 14 4 0.010 None 1.000 1 2019 2019
CUI: C0149887
Disease: Slipped Capital Femoral Epiphyses
Slipped Capital Femoral Epiphyses 		disease Musculoskeletal Diseases Disease or Syndrome 15 0.010 None 1.000 1 2018 2018
CUI: C0795953
Disease: MASA SYNDROME (disorder)
MASA SYNDROME (disorder) 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 16 13 0.010 None 1.000 1 1995 1995
CUI: C0233705
Disease: Cancerophobia
Cancerophobia 		disease Mental Disorders Mental or Behavioral Dysfunction 17 0.010 None 1.000 1 2018 2018
CUI: C0340493
Disease: Paroxysmal familial ventricular fibrillation
Paroxysmal familial ventricular fibrillation 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 18 5 0.010 None 1.000 1 2019 2019
CUI: C1504431
Disease: Idiopathic pneumonia syndrome
Idiopathic pneumonia syndrome 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 18 0.010 None 1.000 1 2018 2018
CUI: C0265216
Disease: X-linked hydrocephalus syndrome
X-linked hydrocephalus syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 20 24 0.020 None 1.000 2 1995 1997
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 22 17 0.100 None 1.000 5 3 2013 2016
CUI: C0152276
Disease: Granulocytic Sarcoma
Granulocytic Sarcoma 		disease Neoplasms Neoplastic Process 28 1 0.010 None 1.000 1 2010 2010
CUI: C1631597
Disease: VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 31 121 0.340 None 1.000 4 2016 2019
CUI: C4316909
Disease: Marijuana Use
Marijuana Use 		disease Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 33 0.010 None 1.000 1 2020 2020