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Disease core ontology applied to Rare Diseases
Last uploaded:
February 7, 2014
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| Id | http://www.limics.org/hrdo/rdfns#pat_id_17985
http://www.limics.org/hrdo/rdfns#pat_id_17985
|
|---|---|
| Preferred Name | Congenital hypogonadotropic hypogonadism |
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| prefLabel |
Congenital hypogonadotropic hypogonadism
|
|---|---|
| prevalence |
1-5 / 10 000
|
| inheritance |
X-linked recessive
Autosomal dominant
Autosomal recessive
|
| id_OMS |
E23.0
|
| prefixIRI |
hrdo:pat_id_17985
|
| id_Orpha |
174590
|
| subClassOf | |
| patType |
group of phenomes
|
| type | |
| id_Medline |
neant
|
| ageOfOnset |
Neonatal/infancy
|
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