Human Phenotype Ontology 
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
Definition:Any abnormality of the eye, including location, spacing, and intraocular abnormalities.
Comments:
Reference:HP:0000478
MSeqDR-LSDB(LS)
& Disease (OMIM):
1. LS OMIM: #203700 MITOCHONDRIAL DNA DEPLETION SYNDROME ..
2.      OMIM: #103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-L..
3.      OMIM: #143880 HYPERCALCEMIA, INFANTILE;;HYPERCALCEM..
4.      OMIM: #160980 CARNEY COMPLEX, TYPE 1; CNC1;;CARNEY ..
5.      OMIM: #184095 SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEA..
6.      OMIM: #184840 STICKLER SYNDROME, TYPE III; STL3;;ST..
7.      OMIM: #202650 AGNATHIA-OTOCEPHALY COMPLEX; AGOTC;;D..
8.      OMIM: #215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; ..
9.      OMIM: #224750 SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS..
10.      OMIM: #246700 CHYLOMICRON RETENTION DISEASE; CMRD;;..
11.      OMIM: #247100 LIPOID PROTEINOSIS OF URBACH AND WIET..

Warning: 10 out of 615 matches reported due to space limit
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       Child Nodes:
........expandAbnormal eye morphology (HP:0012372) help
........expandAbnormal eye physiology (HP:0012373) help

 Sister Nodes: 
..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 abdomen (HP:0001438) help
..expandAbnormality of the breast (HP:0000769) help
..expandAbnormality of the cardiovascular system (HP:0001626) 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
..expandGrowth abnormality (HP:0001507) help
..expandNeoplasm (HP:0002664) help
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium.