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.
6q24-Related Transient Neonatal Diabetes Mellitus
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
Paternal uniparental disomy of chromosome 6
disease Disease or Syndrome 2 0.300 None 0
CUI: C0404531
Disease: Hypertrophy of labia
Hypertrophy of labia
phenotype Pathologic Function 4 0.100 None 0
CUI: C1306893
Disease: Anomaly of placenta
Anomaly of placenta
phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 5 0.100 None 0
Abnormality of the pancreatic islet cells
disease Anatomical Abnormality 6 0.100 None 0
CUI: C4021808
Disease: Abnormality of earlobe
Abnormality of earlobe
disease Anatomical Abnormality 9 1 0.100 None 0
Neonatal insulin-dependent diabetes mellitus
phenotype Finding 10 6 0.100 None 0
CUI: C1859455
Disease: Small anterior fontanelle
Small anterior fontanelle
phenotype Finding 11 4 0.100 None 0
Diabetes Mellitus, Transient Neonatal, 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 12 11 0.520 None 1.000 4 2000 2011
Contractures of the joints of the lower limbs
phenotype Finding 12 3 0.100 None 0
CUI: C1855514
Disease: Severe failure to thrive
Severe failure to thrive
phenotype Finding 14 4 0.100 None 0
CUI: C1865244
Disease: Shallow orbits
Shallow orbits
phenotype Eye Diseases Finding 20 4 0.100 None 0
Transient neonatal diabetes mellitus
disease Disease or Syndrome 23 0.140 None 1.000 4 2001 2014
CUI: C0162275
Disease: Ketonuria
Ketonuria
disease Nutritional and Metabolic Diseases Disease or Syndrome 26 1 0.100 None 0
CUI: C1856786
Disease: Hypoplastic fingernail
Hypoplastic fingernail
phenotype Finding 30 2 0.100 None 0
CUI: C0038238
Disease: Steatorrhea
Steatorrhea
phenotype Digestive System Diseases; Nutritional and Metabolic Diseases Finding 37 0.100 None 0
CUI: C0546884
Disease: Hypovolemia
Hypovolemia
phenotype Pathological Conditions, Signs and Symptoms Finding 37 3 0.100 None 0
CUI: C1857949
Disease: Prominent metopic ridge
Prominent metopic ridge
phenotype Finding 39 2 0.100 None 0
CUI: C1865916
Disease: Bilateral ptosis
Bilateral ptosis
phenotype Eye Diseases Finding 50 14 0.100 None 0
CUI: C0017979
Disease: Glycosuria
Glycosuria
phenotype Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 53 7 0.100 None 0
CUI: C1853737
Disease: Prominent occiput
Prominent occiput
phenotype Finding 53 1 0.100 None 0
CUI: C0151747
Disease: Renal tubular disorder
Renal tubular disorder
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 64 5 0.100 None 0
CUI: C4281993
Disease: Neonatal respiratory distress
Neonatal respiratory distress
phenotype Respiratory Tract Diseases Finding 64 34 0.100 None 0
CUI: C3463897
Disease: HYDATIDIFORM MOLE, RECURRENT, 1
HYDATIDIFORM MOLE, RECURRENT, 1
disease Disease or Syndrome 66 14 0.020 None 1.000 2 2002 2010
CUI: C0426415
Disease: Large nose
Large nose
phenotype Finding 70 7 0.100 None 0