Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024
Preferred Name

Congenital adrenal hyperplasia
Synonyms

CAH

Definitions

A group of rare inherited endocrine disorders caused by a steroidogenic enzyme deficiency and characterized by adrenal insufficiency and variable degrees of hyper- or hypoandrogenism manifestations, depending on disease type and severity.

ID

http://www.orpha.net/ORDO/Orphanet_418

alternative_term

CAH

definition

A group of rare inherited endocrine disorders caused by a steroidogenic enzyme deficiency and characterized by adrenal insufficiency and variable degrees of hyper- or hypoandrogenism manifestations, depending on disease type and severity.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=418

has_inheritance

Autosomal recessive

hasDbXref

ICD-10:E25.0

OMIM:201910

OMIM:613571

ICD-11:5A71.01

OMIM:201710

MedDRA:10010323

OMIM:202010

OMIM:201810

OMIM:202110

MeSH:D000312

UMLS:C0001627

label

Congenital adrenal hyperplasia

notation

Clinical group

ORPHA:418

prefixIRI

ORDO:Orphanet_418

prefLabel

Congenital adrenal hyperplasia

present_in

Czech Republic AND has_birth_prevalence_average_value : 7.98 AND has_birth_prevalence_range : 1-9 / 100 000

Belgium AND has_birth_prevalence_average_value : 4.0 AND has_birth_prevalence_range : 1-9 / 100 000

New Zealand AND has_birth_prevalence_average_value : 6.9 AND has_birth_prevalence_range : 1-9 / 100 000

Taiwan, Province of China AND has_birth_prevalence_average_value : 6.7 AND has_birth_prevalence_range : 1-9 / 100 000

Cuba AND has_birth_prevalence_average_value : 6.3 AND has_birth_prevalence_range : 1-9 / 100 000

Europe AND has_birth_prevalence_average_value : 6.7 AND has_birth_prevalence_range : 1-9 / 100 000

Switzerland AND has_birth_prevalence_average_value : 9.3 AND has_birth_prevalence_range : 1-9 / 100 000

Netherlands AND has_birth_prevalence_average_value : 7.65 AND has_birth_prevalence_range : 1-9 / 100 000

Sweden AND has_birth_prevalence_average_value : 10.2 AND has_birth_prevalence_range : 1-5 / 10 000

United States AND has_birth_prevalence_average_value : 4.8 AND has_birth_prevalence_range : 1-9 / 100 000

France AND has_birth_prevalence_average_value : 8.6 AND has_birth_prevalence_range : 1-9 / 100 000

Germany AND has_birth_prevalence_average_value : 12.8 AND has_birth_prevalence_range : 1-5 / 10 000

India AND has_birth_prevalence_average_value : 38.8 AND has_birth_prevalence_range : 1-5 / 10 000

Japan AND has_birth_prevalence_average_value : 5.35 AND has_birth_prevalence_range : 1-9 / 100 000

United Kingdom AND has_birth_prevalence_average_value : 5.6 AND has_birth_prevalence_range : 1-9 / 100 000

Europe AND has_point_prevalence_average_value : 10.0 AND has_point_prevalence_range : 1-9 / 100 000

Europe AND has_annual_incidence_average_value : 13.35 AND has_annual_incidence_range : 1-5 / 10 000

Italy AND has_birth_prevalence_average_value : 6.65 AND has_birth_prevalence_range : 1-9 / 100 000

China AND has_point_prevalence_average_value : 1.36 AND has_point_prevalence_range : 1-9 / 100 000

subClassOf

http://www.orpha.net/ORDO/Orphanet_156643

http://www.orpha.net/ORDO/Orphanet_90692

http://www.orpha.net/ORDO/Orphanet_181412

http://www.orpha.net/ORDO/Orphanet_101960

http://www.orpha.net/ORDO/Orphanet_557492

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Delete Mapping To Ontology Source
http://www.orpha.net/ORDO/Orphanet_418 CCONT SAME_URI
http://www.orpha.net/ORDO/Orphanet_418 EFO SAME_URI
http://www.orpha.net/ORDO/Orphanet_418 EFO SAME_URI
http://pat.nichd.nih.gov/maternalconditions/C0001627 PATMHC LOOM
http://www.co-ode.org/ontologies/galen#CongenitalAdrenalHyperplasia GALEN LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0001627 OCHV LOOM
http://purl.obolibrary.org/obo/MONDO_0018479 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0018479 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0018479 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0018479 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0018479 DOVES LOOM
http://purl.jp/bio/4/id/200906090671453439 IOBC LOOM
http://purl.bioontology.org/ontology/MEDDRA/10010323 MEDDRA LOOM
http://purl.obolibrary.org/obo/HP_0008258 HP LOOM
http://purl.obolibrary.org/obo/HP_0008258 UPHENO LOOM
http://www.limics.org/hrdo/rdfns#pat_id_648 HRDO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34360 NCIT LOOM
rgo:27861 GAMUTS LOOM
http://purl.obolibrary.org/obo/DOID_0050811 DTO LOOM
http://purl.obolibrary.org/obo/DOID_0050811 DOID LOOM
http://purl.obolibrary.org/obo/DOID_0050811 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_0050811 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_0050811 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0050811 FNS-H LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU014663 OMIM LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/237751000 SNOMEDCT LOOM
http://purl.obolibrary.org/obo/DERMO_0001521 DERMO LOOM
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Adrenal_Hyperplasia PEDTERM LOOM
http://purl.bioontology.org/ontology/LNC/LA12533-8 LOINC LOOM
http://purl.bioontology.org/ontology/CSP/0060-3730 CRISP LOOM
http://www.phoc.org.cn/pmo/class/PMO_00006212 PMAPP-PMO LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0001627 MEDLINEPLUS LOOM
http://purl.bioontology.org/ontology/MESH/D000312 GSSO LOOM
http://purl.obolibrary.org/obo/NCIT_C34360 BERO LOOM
http://purl.obolibrary.org/obo/DOID_12255 CLO LOOM
http://purl.bioontology.org/ontology/RCD/X40MT RCD LOOM
http://purl.bioontology.org/ontology/LNC/LP56767-4 LOINC LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_12255 NATPRO LOOM
http://nanbyodata.jp/ontology/NANDO_2100134 NANDO LOOM
http://localhost/plosthes.2017-1#7455 PLOSTHES LOOM
http://purl.bioontology.org/ontology/LNC/MTHU021596 LOINC LOOM
http://www.gamuts.net/entity#congenital_adrenal_hyperplasia GAMUTS REST