Human Phenotype Ontology / 人类表型本体

Last uploaded: September 7, 2023
Preferred Name

Corneal dystrophy

Definitions

The term corneal dystrophy embraces a heterogenous group of bilateral genetically determined non-inflammatory corneal diseases that are restricted to the cornea.

ID

http://purl.obolibrary.org/obo/HP_0001131

database_cross_reference

UMLS:C0010036

SNOMEDCT_US:5587004

definition

The term corneal dystrophy embraces a heterogenous group of bilateral genetically determined non-inflammatory corneal diseases that are restricted to the cornea.

has_alternative_id

HP:0007775

HP:0008005

has_obo_namespace

human_phenotype

id

HP:0001131

in_subset

http://purl.obolibrary.org/obo/hp.obo#hposlim_core

label

Corneal dystrophy

notation

HP:0001131

prefLabel

Corneal dystrophy

treeView

http://purl.obolibrary.org/obo/HP_0000481

subClassOf

http://purl.obolibrary.org/obo/HP_0000481

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http://purl.obolibrary.org/obo/DOID_2566 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_2566 Human Disease Ontology / 人类疾病本体 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34513 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU015719 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://www.orpha.net/ORDO/Orphanet_34533 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0018102 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0018102 Experimental Factor Ontology / 实验性因素本体 LOOM