Human Phenotype Ontology / 人类表型本体

Last uploaded: September 7, 2023
Preferred Name

Retinal atrophy

Definitions

Well-demarcated area(s) of partial or complete depigmentation in the fundus, reflecting atrophy of the retinal pigment epithelium with associated retinal photoreceptor loss.

ID

http://purl.obolibrary.org/obo/HP_0001105

database_cross_reference

SNOMEDCT_US:95695004

SNOMEDCT_US:405722004

UMLS:C0521694

UMLS:C0035304

MSH:D012162

definition

Well-demarcated area(s) of partial or complete depigmentation in the fundus, reflecting atrophy of the retinal pigment epithelium with associated retinal photoreceptor loss.

has_obo_namespace

human_phenotype

id

HP:0001105

label

Retinal atrophy

notation

HP:0001105

prefLabel

Retinal atrophy

treeView

http://purl.obolibrary.org/obo/HP_0000546

subClassOf

http://purl.obolibrary.org/obo/HP_0000546

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http://purl.bmicc.cn/ontology/ICD11CN/9B78.9 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM
http://purl.obolibrary.org/obo/HP_0001105 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/HP_0001105 Experimental Factor Ontology / 实验性因素本体 SAME_URI
http://purl.bioontology.org/ontology/OMIM/MTHU000323 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM