Human Phenotype Ontology / 人类表型本体

Last uploaded: September 7, 2023
Preferred Name

Skeletal dysplasia

Synonyms

Abnormal skeletal development

Definitions

A general term describing features characterized by abnormal development of bones and connective tissues. The word skeletal dysplasia is most often used to describe a group of over 380 inherited conditions that involve abnormal development of bones and connective tissues. However, the word can also be used to describe the presence of congenital defects of bones or connective tissues that are found in one or more of the diseases, especially on prenatal ultrasound, i.e., a situation in which it is often not yet possible to make an exact etiological diagnosis. This is the sense of the phrase we use in the HPO. It is, however, preferable to annotate the observed abnormalities.

ID

http://purl.obolibrary.org/obo/HP_0002652

comment

The word skeletal dysplasia is most often used to describe a group of over 380 inherited conditions that involve abnormal development of bones and connective tissues. However, the word can also be used to describe the presence of congenital defects of bones or connective tissues that are found in one or more of the diseases, especially on prenatal ultrasound, i.e., a situation in which it is often not yet possible to make an exact etiological diagnosis. This is the sense of the phrase we use in the HPO. It is, however, preferable to annotate the observed abnormalities.

database_cross_reference

UMLS:C4280567

MSH:D010009

SNOMEDCT_US:240190009

SNOMEDCT_US:105985007

UMLS:C0029422

definition

A general term describing features characterized by abnormal development of bones and connective tissues.

has_alternative_id

HP:0005685

has_broad_synonym

Abnormal skeletal development

has_obo_namespace

human_phenotype

id

HP:0002652

label

Skeletal dysplasia

notation

HP:0002652

prefLabel

Skeletal dysplasia

treeView

http://purl.obolibrary.org/obo/HP_0011842

subClassOf

http://purl.obolibrary.org/obo/HP_0011842

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http://purl.obolibrary.org/obo/HP_0002652 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.obolibrary.org/obo/HP_0002652 Human Disease Ontology / 人类疾病本体 SAME_URI
http://purl.obolibrary.org/obo/HP_0002652 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/HP_0002652 Experimental Factor Ontology / 实验性因素本体 SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018230 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0018230 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU042509 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM