WNT4, Wnt family member 4, 54361

N. diseases: 135; N. variants: 14
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: C0239234
Disease: Low set ears
Low set ears
disease Congenital Abnormality 489 64 0.100 None 0
CUI: C0265783
Disease: Congenital hypoplasia of lung
Congenital hypoplasia of lung
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Congenital Abnormality 175 6 0.100 None 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Congenital Abnormality 27 0.100 None 0
CUI: C0456070
Disease: Growth delay
Growth delay
phenotype Pathologic Function 244 40 0.100 None 0
CUI: C0431447
Disease: Synophrys
Synophrys
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 111 23 0.100 None 0
CUI: C0266273
Disease: Congenital absence of adrenal gland
Congenital absence of adrenal gland
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Endocrine System Diseases Congenital Abnormality 2 0.100 None 0
CUI: C0349588
Disease: Short stature
Short stature
phenotype Finding 1127 292 0.100 None 0
Congenital absence of kidneys syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 110 0.100 None 0
CUI: C1834124
Disease: Shield chest
Shield chest
phenotype Finding 12 2 0.100 None 0
CUI: C3276036
Disease: High anterior hairline
High anterior hairline
phenotype Finding 25 3 0.100 None 0
CUI: C4021610
Disease: Bilateral lung agenesis
Bilateral lung agenesis
disease Anatomical Abnormality 3 0.100 None 0
CUI: C4021794
Disease: Abnormality of the adrenal glands
Abnormality of the adrenal glands
disease Anatomical Abnormality 10 0.100 None 0
CUI: C4021813
Disease: Oral cleft
Oral cleft
disease Congenital Abnormality 85 28 0.100 None 0
CUI: C4021818
Disease: Abnormality of the ovary
Abnormality of the ovary
disease Anatomical Abnormality 8 1 0.100 None 0
CUI: C4022995
Disease: Sex reversal
Sex reversal
phenotype Finding 14 0.100 None 0
Aplasia/Hypoplasia of the fallopian tube
phenotype Finding 2 0.100 None 0
CUI: C4072885
Disease: Increased serum testosterone level
Increased serum testosterone level
phenotype Finding 5 1 0.100 None 0
CUI: C1841990
Disease: Aplasia of the vagina
Aplasia of the vagina
phenotype Finding 2 0.100 None 0
CUI: C1956257
Disease: Pulmonary Stenosis
Pulmonary Stenosis
disease Cardiovascular Diseases Disease or Syndrome 106 40 0.100 None 0
CUI: C1850041
Disease: Facial hirsutism
Facial hirsutism
phenotype Finding 4 2 0.100 None 0
CUI: C1853487
Disease: Thick eyebrow
Thick eyebrow
phenotype Finding 104 13 0.100 None 0
CUI: C1855285
Disease: Protruding ear
Protruding ear
phenotype Finding 152 6 0.100 None 0
CUI: C1855335
Disease: Hypoplasia of the bladder
Hypoplasia of the bladder
phenotype Finding 4 0.100 None 0
CUI: C1856023
Disease: Abnormal vagina morphology
Abnormal vagina morphology
phenotype Finding 12 0.100 None 0
CUI: C1860244
Disease: Malrotation of small bowel
Malrotation of small bowel
phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Finding 7 0.100 None 0