Human Phenotype Ontology

Last uploaded: April 26, 2024
Preferred Name

Skeletal dysplasia

Synonyms

Abnormal skeletal development

Definitions

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

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

MSH:D010009

SNOMEDCT_US:105985007

UMLS:C4280567

UMLS:C0029422

SNOMEDCT_US:240190009

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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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/HP_0002652 EFO SAME_URI
http://purl.obolibrary.org/obo/HP_0002652 DOID SAME_URI
http://purl.obolibrary.org/obo/HP_0002652 MAXO SAME_URI
http://purl.obolibrary.org/obo/HP_0002652 OBA SAME_URI
http://purl.obolibrary.org/obo/HP_0002652 GAMUTS SAME_URI
http://purl.obolibrary.org/obo/HP_0002652 HHEAR SAME_URI
http://purl.obolibrary.org/obo/HP_0002652 UPHENO SAME_URI
http://purl.obolibrary.org/obo/HP_0002652 NIFSTD SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018230 EFO LOOM
http://purl.obolibrary.org/obo/HP_0002652 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0018230 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0018230 OBA LOOM
http://purl.obolibrary.org/obo/HP_0002652 OBA LOOM
http://purl.obolibrary.org/obo/HP_0002652 DOID LOOM
http://purl.obolibrary.org/obo/HP_0002652 MAXO LOOM
http://purl.obolibrary.org/obo/MONDO_0018230 GCBO LOOM
http://purl.obolibrary.org/obo/MONDO_0018230 DOVES LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0410528 OCHV LOOM
http://www.phoc.org.cn/pmo/class/PMO_00013956 PMAPP-PMO LOOM
http://purl.obolibrary.org/obo/HP_0002652 HHEAR LOOM
http://purl.obolibrary.org/obo/HP_0002652 UPHENO LOOM
http://purl.obolibrary.org/obo/HP_0002652 NIFSTD LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/105986008 SNOMEDCT LOOM
http://radlex.org/RID/RID34679 RADLEX LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#32821 OCHV LOOM
http://www.semanticweb.org/ontologies/2012/5/Ontology1338526551855.owl#Skeletal_dysplasia RPO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10072610 MEDDRA LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU042509 OMIM LOOM
http://purl.bioontology.org/ontology/RCD/X70BZ RCD LOOM
http://purl.org/obo/owl/HP#HP_0002652 BDO LOOM
http://www.gamuts.net/entity#skeletal_dysplasia GAMUTS LOOM
http://www.gamuts.net/entity#skeletal_dysplasia GAMUTS REST