Human Phenotype Ontology 
..Starting node
..expand
All (HP:0000001)help
Term ID: 1
Name: All
Synonym:
Definition:
Comments:
Reference: HP:0000001
Genes and Diseases:There are 16290 terms for your input, too many to show detail here. Please try its child terms.
 
       Child Nodes:
........expandMode of inheritance (HP:0000005) help
................... HP:0000006 Autosomal dominant inheritance
................... HP:0000007 Autosomal recessive inheritance
................... HP:0001425 Heterogeneous
................... HP:0001426 Multifactorial inheritance
................... HP:0001427 Mitochondrial inheritance
................... HP:0001428 Somatic mutation
................... HP:0001466 Contiguous gene syndrome
................... HP:0001472 Familial predisposition
................... HP:0003743 Genetic anticipation
................... HP:0003745 Sporadic
................... HP:0010985 Gonosomal inheritance
........expandPhenotypic abnormality (HP:0000118) help
................... HP:0000119 Abnormality of the genitourinary system
................... HP:0000152 Abnormality of head or neck
................... HP:0000478 Abnormality of the eye
................... HP:0000598 Abnormality of the ear
................... HP:0000707 Abnormality of the nervous system
................... HP:0000769 Abnormality of the breast
................... HP:0000818 Abnormality of the endocrine system
................... HP:0000924 Abnormality of the skeletal system
................... HP:0001197 Abnormality of prenatal development or birth
................... HP:0001507 Growth abnormality
................... HP:0001574 Abnormality of the integument
................... HP:0001608 Abnormality of the voice
................... HP:0001626 Abnormality of the cardiovascular system
................... HP:0001871 Abnormality of blood and blood-forming tissues
................... HP:0001939 Abnormality of metabolism/homeostasis
................... HP:0002086 Abnormality of the respiratory system
................... HP:0002664 Neoplasm
................... HP:0002715 Abnormality of the immune system
................... HP:0003011 Abnormality of the musculature
................... HP:0003549 Abnormality of connective tissue
................... HP:0025031 Abnormality of the digestive system
................... HP:0025142 Constitutional symptom
................... HP:0025354 Abnormal cellular phenotype
................... HP:0040064 Abnormality of limbs
................... HP:0045027 Abnormality of the thoracic cavity
................... HP:0500014 Abnormal test result
........expandClinical modifier (HP:0012823) help
................... HP:0003812 Phenotypic variability
................... HP:0012824 Severity
................... HP:0012830 Position
................... HP:0025204 Triggered by
................... HP:0025254 Ameliorated by
................... HP:0025280 Pain characteristic
................... HP:0025285 Aggravated by
................... HP:0031375 Refractory
........expandClinical course (HP:0031797) help
................... HP:0003674 Onset
................... HP:0003679 Pace of progression
................... HP:0011008 Temporal pattern
................... HP:0040006 Mortality/Aging
........expandFrequency (HP:0040279) help
................... HP:0040280 Obligate
................... HP:0040281 Very frequent
................... HP:0040282 Frequent
................... HP:0040283 Occasional
................... HP:0040284 Very rare
................... HP:0040285 Excluded

 Sister Nodes: 


Genes (0) :

Diseases (0) :
 

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