Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024
Preferred Name

Hypochondrogenesis
Synonyms
ID

http://www.orpha.net/ORDO/Orphanet_93297

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=93297

has_age_of_onset

Infancy

Neonatal

has_inheritance

Autosomal dominant

hasDbXref

ICD-11:LD24.51

OMIM:200610

MeSH:C563007

ICD-10:Q77.0

UMLS:C0542428

label

Hypochondrogenesis

notation

ORPHA:93297

Clinical subtype

part_of

http://www.orpha.net/ORDO/Orphanet_93421

http://www.orpha.net/ORDO/Orphanet_932

prefixIRI

ORDO:Orphanet_93297

prefLabel

Hypochondrogenesis

present_in

Worldwide AND has_point_prevalence_range : Unknown

treeView

http://www.orpha.net/ORDO/Orphanet_93421

http://www.orpha.net/ORDO/Orphanet_932

subClassOf

http://www.orpha.net/ORDO/Orphanet_557494

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