CDC73, cell division cycle 73, 79577

N. diseases: 144; N. variants: 31
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: C1840402
Disease: HYPERPARATHYROIDISM 1
HYPERPARATHYROIDISM 1
disease Endocrine System Diseases Disease or Syndrome 1 6 0.700 strong 1.000 6 5 2002 2019
CUI: C0346253
Disease: Cortical adenoma of kidney
Cortical adenoma of kidney
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 1 0.100 None 0
CUI: C1840403
Disease: Parathyroid Adenoma, Familial
Parathyroid Adenoma, Familial
disease Endocrine System Diseases Disease or Syndrome 1 0.300 None 0
CUI: C4017087
Disease: CYSTIC PARATHYROID ADENOMA, SOMATIC
CYSTIC PARATHYROID ADENOMA, SOMATIC
disease Finding 1 1 0.100 None 0 1
CUI: C0278681
Disease: metastatic parathyroid cancer
metastatic parathyroid cancer
disease Neoplasms; Endocrine System Diseases Neoplastic Process 2 1 0.010 None 1.000 1 2020 2020
CUI: C0278684
Disease: recurrent parathyroid cancer
recurrent parathyroid cancer
disease Neoplasms; Endocrine System Diseases Neoplastic Process 2 0.010 None 1.000 1 2018 2018
CUI: C4072940
Disease: Ossifying fibroma of the jaw
Ossifying fibroma of the jaw
disease Neoplasms; Stomatognathic Diseases Neoplastic Process 2 2 0.110 None 1.000 1 2 2017 2017
CUI: C1840396
Disease: Renal hamartoma
Renal hamartoma
phenotype Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Pathologic Function 2 0.100 None 0
CUI: C2675664
Disease: PARATHYROID ADENOMA, SOMATIC
PARATHYROID ADENOMA, SOMATIC
disease Finding 2 2 0.100 None 0 1
CUI: C4552061
Disease: Mandibular pain
Mandibular pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 2 0.100 None 0
Benign mixed epithelial and stromal tumor of kidney
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 3 0.010 None 1.000 1 2019 2019
CUI: C4054076
Disease: Renal Angiomyoadenomatous Tumor
Renal Angiomyoadenomatous Tumor
disease Neoplastic Process 3 0.010 None 1.000 1 2015 2015
CUI: C1305409
Disease: Atypical adenoma
Atypical adenoma
disease Neoplasms Neoplastic Process 5 1 0.040 None 1.000 4 2006 2019
CUI: C0475732
Disease: Hypercalcemia, Infantile
Hypercalcemia, Infantile
phenotype Nutritional and Metabolic Diseases Finding 5 0.100 None 0
CUI: C0236000
Disease: Jaw pain
Jaw pain
phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Stomatognathic Diseases Sign or Symptom 6 1 0.100 None 0
CUI: C0271846
Disease: Familial hyperparathyroidism
Familial hyperparathyroidism
disease Endocrine System Diseases Disease or Syndrome 7 1 0.090 None 1.000 9 2007 2020
CUI: C0042065
Disease: Genitourinary Neoplasms
Genitourinary Neoplasms
group Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 9 1 0.010 None 1.000 1 2020 2020
CUI: C4021812
Disease: Abnormality of the head
Abnormality of the head
disease Anatomical Abnormality 9 0.100 None 0
Familial Isolated Hyperparathyroidism
disease Endocrine System Diseases Disease or Syndrome 10 4 0.600 None 0.967 30 1 1993 2020
CUI: C1336750
Disease: Thyroid Gland Oncocytic Adenoma
Thyroid Gland Oncocytic Adenoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 11 0.100 None 0
Hyperparathyroidism-Jaw Tumor Syndrome
disease Neoplasms; Musculoskeletal Diseases; Endocrine System Diseases; Stomatognathic Diseases Neoplastic Process 12 7 0.800 definitive 1.000 76 6 1990 2020
Malignant tumor of parathyroid gland
disease Neoplasms; Endocrine System Diseases Neoplastic Process 13 1 0.080 None 1.000 8 1 1993 2013
CUI: C0151879
Disease: Shortened QT interval
Shortened QT interval
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Finding 13 0.100 None 0
CUI: C4551680
Disease: Generalized osteoporosis
Generalized osteoporosis
disease Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 13 0.100 None 0
CUI: C0745106
Disease: hyperparathyroid
hyperparathyroid
disease Disease or Syndrome 14 0.010 None 1.000 1 2019 2019