TCMBANKDI002275 |
|
- |
Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system |
Disease or Syndrome |
phenotype |
TCMBANKDI002742 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
Abnormality of the genitourinary system |
Disease or Syndrome |
group |
TCMBANKDI004086 |
|
Nutritional and Metabolic Diseases |
Abnormality of metabolism/homeostasis |
Disease or Syndrome |
disease |
TCMBANKDI004967 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
- |
Disease or Syndrome |
disease |
TCMBANKDI007439 |
|
- |
- |
Finding |
disease |
TCMBANKDI008598 |
|
- |
Abnormality of the ear |
Finding |
phenotype |
TCMBANKDI011209 |
|
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system |
Finding |
phenotype |
TCMBANKDI012986 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases |
- |
Disease or Syndrome |
disease |
TCMBANKDI018731 |
|
Digestive System Diseases |
Abnormality of the digestive system |
Disease or Syndrome |
disease |
TCMBANKDI019157 |
|
- |
Abnormality of the genitourinary system |
Finding |
phenotype |
TCMBANKDI019650 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
- |
Disease or Syndrome |
phenotype |
TCMBANKDI020079 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
- |
Disease or Syndrome |
disease |
TCMBANKDI023751 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
Abnormality of the musculature |
Finding |
phenotype |
TCMBANKDI025832 |
|
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
Abnormality of the respiratory system |
Sign or Symptom |
phenotype |
TCMBANKDI028918 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
Abnormality of the genitourinary system |
Finding |
phenotype |