POMC, proopiomelanocortin, 5443

N. diseases: 873; N. variants: 39
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: C4727593
Disease: Crooke Cell Adenoma
Crooke Cell Adenoma
disease Neoplasms; Nervous System Diseases; Endocrine System Diseases Neoplastic Process 1 0.020 None 1.000 2 2018 2019
CUI: C0021177
Disease: Increased Libido
Increased Libido
phenotype Sign or Symptom 1 0.010 None 1.000 1 2018 2018
CUI: C0154695
Disease: Diplegic Infantile Cerebral Palsy
Diplegic Infantile Cerebral Palsy
disease Nervous System Diseases Disease or Syndrome 1 0.300 None 1.000 1 1997 1997
Cerebral Palsy, Quadriplegic, Infantile
disease Nervous System Diseases Disease or Syndrome; Congenital Abnormality 1 0.300 None 1.000 1 1997 1997
CUI: C0154698
Disease: Monoplegic Infantile Cerebral Palsy
Monoplegic Infantile Cerebral Palsy
disease Nervous System Diseases Disease or Syndrome 1 0.300 None 1.000 1 1997 1997
CUI: C0264725
Disease: Acute left-sided heart failure
Acute left-sided heart failure
disease Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C0270807
Disease: Monoplegic Cerebral Palsy
Monoplegic Cerebral Palsy
disease Nervous System Diseases Disease or Syndrome 1 0.300 None 1.000 1 1997 1997
CUI: C0394003
Disease: Cerebral Palsy, Dystonic-Rigid
Cerebral Palsy, Dystonic-Rigid
disease Nervous System Diseases Disease or Syndrome 1 0.300 None 1.000 1 1997 1997
CUI: C0394007
Disease: Cerebral Palsy, Atonic
Cerebral Palsy, Atonic
disease Nervous System Diseases Disease or Syndrome 1 0.300 None 1.000 1 1997 1997
CUI: C0549471
Disease: Pancoast Tumor
Pancoast Tumor
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 1 0.010 None 1.000 1 2017 2017
CUI: C0745261
Disease: Infantile apnea
Infantile apnea
disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Disease or Syndrome 1 0.010 None 1.000 1 1987 1987
CUI: C0751024
Disease: Cerebral Palsy, Mixed
Cerebral Palsy, Mixed
disease Nervous System Diseases Disease or Syndrome 1 0.300 None 1.000 1 1997 1997
CUI: C0751025
Disease: Cerebral Palsy, Rolandic Type
Cerebral Palsy, Rolandic Type
disease Nervous System Diseases Disease or Syndrome 1 0.300 None 1.000 1 1997 1997
CUI: C0751141
Disease: Facial Palsy, Upper Motor Neuron
Facial Palsy, Upper Motor Neuron
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases Sign or Symptom 1 0.300 None 1.000 1 1971 1971
CUI: C0751142
Disease: Facial Palsy, Lower Motor Neuron
Facial Palsy, Lower Motor Neuron
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases Sign or Symptom 1 0.300 None 1.000 1 1971 1971
CUI: C0751143
Disease: Hemifacial Paralysis
Hemifacial Paralysis
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases Sign or Symptom 1 0.300 None 1.000 1 1971 1971
CUI: C0852698
Disease: 17,20-desmolase deficiency
17,20-desmolase deficiency
disease Disease or Syndrome 1 0.010 None 1.000 1 1989 1989
CUI: C0871007
Disease: snake phobia
snake phobia
disease Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2017 2017
CUI: C1096560
Disease: Infection caused by Malassezia
Infection caused by Malassezia
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C2936444
Disease: Pyogenic Sacroiliitis
Pyogenic Sacroiliitis
disease Musculoskeletal Diseases Disease or Syndrome 1 0.300 None 1.000 1 2010 2010
CUI: C2936445
Disease: Septic Sacroiliitis
Septic Sacroiliitis
disease Musculoskeletal Diseases Disease or Syndrome 1 0.300 None 1.000 1 2010 2010
CUI: C3888993
Disease: Hypocortisolaemia
Hypocortisolaemia
disease Disease or Syndrome 1 1 0.010 None 1.000 1 2019 2019
CUI: C4087197
Disease: Ectopic posterior pituitary gland
Ectopic posterior pituitary gland
disease Disease or Syndrome 1 0.010 None 1.000 1 2014 2014
OBESITY, EARLY-ONSET, SUSCEPTIBILITY TO
phenotype Finding 1 1 0.100 None 0 1
CUI: C4285817
Disease: Cortisol deficiency
Cortisol deficiency
disease Disease or Syndrome 2 0.090 None 0.889 9 1991 2019