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 eye (HP:0000478)help
Term ID: 478
Name: Abnormality of the eye
Synonym: Abnormal eye; Abnormality of the eye; Eye disease
Definition: Any abnormality of the eye, including location, spacing, and intraocular abnormalities.
Comments:
Reference: HP:0000478
Genes and Diseases:There are 1114 terms for your input, too many to show detail here. Please try its child terms.
 
       Child Nodes:
......expandAbnormal eye morphology (HP:0012372)help
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HP:0012374 Abnormal globe morphology
................... HP:0100012 Neoplasm of the eye
......expandAbnormal eye physiology (HP:0012373)help
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HP:0000496 Abnormality of eye movement
................... HP:0000501 Glaucoma
................... HP:0000504 Abnormality of vision
................... HP:0000508 Ptosis
................... HP:0000539 Abnormality of refraction
................... HP:0000632 Lacrimation abnormality
................... HP:0007686 Abnormal pupillary function
................... HP:0011885 Hemorrhage of the eye
................... HP:0012632 Abnormal intraocular pressure
................... HP:0025401 Staring gaze
................... HP:0025590 Abnormal extraocular muscle physiology
................... HP:0030453 Abnormal visual electrophysiology
................... HP:0030637 Cone dysfunction syndrome
................... HP:0030800 Abnormal visual accommodation
................... HP:0031590 Asthenopia
................... HP:0031879 Abnormal eyelid physiology
................... HP:0100533 Inflammatory abnormality of the eye
................... HP:0200026 Ocular pain

 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 genitourinary system (HP:0000119) 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 June 2019 release.