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: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism
disease Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 41 12 0.200 None 0
CUI: C0271577
Disease: Isolated gonadotropin deficiency
Isolated gonadotropin deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 8 0.200 None 0
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 69 4 0.200 None 0
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 86 30 0.200 None 0
Isolated deficiency of pituitary hormone
disease Disease or Syndrome 8 0.200 None 0
Necrosis of pituitary gland (postpartum)
phenotype Pathologic Function 8 0.200 None 0
CUI: C2874190
Disease: Pituitary short stature
Pituitary short stature
disease Disease or Syndrome 8 0.200 None 0
Idiopathic growth hormone deficiency
disease Disease or Syndrome 10 0.200 None 0
CUI: C0242342
Disease: Sheehan Syndrome
Sheehan Syndrome
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 16 2 0.200 None 0
CUI: C0221405
Disease: Pituitary cachexia
Pituitary cachexia
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 8 0.200 None 0
Isolated lutropin deficiency (disorder)
disease Endocrine System Diseases Disease or Syndrome 9 6 0.200 None 0
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 73 23 0.200 None 0
CUI: C1859014
Disease: Primary gonadal insufficiency
Primary gonadal insufficiency
phenotype Finding 21 0.100 None 0
CUI: C1858574
Disease: Sparse axillary hair
Sparse axillary hair
phenotype Finding 39 0.100 None 0
Increased circulating gonadotropin level
phenotype Nervous System Diseases; Endocrine System Diseases Finding 34 0.100 None 0
CUI: C1858573
Disease: Sparse pubic hair
Sparse pubic hair
phenotype Finding 42 0.100 None 0
CUI: C0241011
Disease: Low serum estradiol levels
Low serum estradiol levels
phenotype Finding 33 0.100 None 0
Female external genitalia in individual with 46,XY karyotype
phenotype Finding 17 1 0.100 None 0
CUI: C0241355
Disease: Small testicle
Small testicle
phenotype Finding 129 0.100 None 0
CUI: C0018418
Disease: Gynecomastia
Gynecomastia
disease Skin and Connective Tissue Diseases Disease or Syndrome 121 8 0.100 None 0
CUI: C0425957
Disease: Secondary amenorrhea
Secondary amenorrhea
phenotype Pathological Conditions, Signs and Symptoms Finding 49 0.100 None 0
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum
phenotype Congenital Abnormality 57 3 0.100 None 0
CUI: C0034012
Disease: Delayed Puberty
Delayed Puberty
phenotype Endocrine System Diseases Pathologic Function 196 21 0.100 None 0
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Disease or Syndrome 988 363 0.100 None 0
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
disease Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 1098 182 0.100 None 0