Human Phenotype Ontology 
Grandparent Node:
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All (HP:0000001)help
Parent Node:
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Phenotypic abnormality (HP:0000118)help
..Starting node
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Abnormality of the genitourinary system (HP:0000119)help
Term ID: 119
Name: Abnormality of the genitourinary system
Synonym: Abnormality of the GU system; Genitourinary abnormality; Genitourinary disease; Genitourinary dysplasia; Genitourinary tract anomalies; Genitourinary tract malformation; Urogenital abnormalities; Urogenital anomalies
Definition: The presence of any abnormality of the genitourinary system.
Comments:
Reference: HP:0000119
Genes and Diseases:There are 1392 terms for your input, too many to show detail here. Please try its child terms.
 
       Child Nodes:
........expandAbnormality of the genital system (HP:0000078) help
................... HP:0000080 Abnormality of reproductive system physiology
................... HP:0010787 Genital neoplasm
................... HP:0012243 Abnormal reproductive system morphology
........expandAbnormality of the urinary system (HP:0000079) help
................... HP:0000809 Urinary tract atresia
................... HP:0010935 Abnormality of the upper urinary tract
................... HP:0010936 Abnormality of the lower urinary tract
................... HP:0011277 Abnormality of the urinary system physiology
........expandNeoplasm of the genitourinary tract (HP:0007379) help
................... HP:0006758 Malignant genitourinary tract tumor
................... HP:0006778 Benign genitourinary tract neoplasm
................... HP:0010786 Urinary tract neoplasm
................... HP:0010787 Genital neoplasm
........expandCloacal abnormality (HP:0012620) help
................... HP:0010475 Cloacal exstrophy
................... HP:0012621 Persistent cloaca
........expandUrogenital fistula (HP:0100589) help
................... HP:0004320 Vaginal fistula
................... HP:0004321 Bladder fistula
................... HP:0004871 Perineal fistula
................... HP:0010480 Urethral fistula
................... HP:0100590 Rectal fistula

 Sister Nodes: 
..expandAbnormal cellular phenotype (HP:0025354) help
..expandAbnormality of blood and blood-forming tissues (HP:0001871) help
..expandAbnormality of connective tissue (HP:0003549) help
..expandAbnormality of head or neck (HP:0000152) help
..expandAbnormality of limbs (HP:0040064) help
..expandAbnormality of metabolism/homeostasis (HP:0001939) help
..expandAbnormality of prenatal development or birth (HP:0001197) help
..expandAbnormality of the breast (HP:0000769) help
..expandAbnormality of the cardiovascular system (HP:0001626) help
..expandAbnormality of the digestive system (HP:0025031) help
..expandAbnormality of the ear (HP:0000598) help
..expandAbnormality of the endocrine system (HP:0000818) help
..expandAbnormality of the eye (HP:0000478) help
..expandAbnormality of the immune system (HP:0002715) help
..expandAbnormality of the integument (HP:0001574) help
..expandAbnormality of the musculature (HP:0003011) help
..expandAbnormality of the nervous system (HP:0000707) help
..expandAbnormality of the respiratory system (HP:0002086) help
..expandAbnormality of the skeletal system (HP:0000924) help
..expandAbnormality of the thoracic cavity (HP:0045027) help
..expandAbnormality of the voice (HP:0001608) help
..expandConstitutional symptom (HP:0025142) help
..expandGrowth abnormality (HP:0001507) help
..expandNeoplasm (HP:0002664) help
..expandobsolete Abnormal test result (HP:0500014) help


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.