Human Disease Ontology

Last uploaded: March 2, 2018
Preferred Name

autosomal dominant disease

Definitions

An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease.

ID

http://purl.obolibrary.org/obo/DOID_0050736

created_by

lschriml

creation_date

2012-07-24T12:51:47Z

definition

An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease.

has_obo_namespace

disease_ontology

id

DOID:0050736

label

autosomal dominant disease

notation

DOID:0050736

prefLabel

autosomal dominant disease

treeView

http://purl.obolibrary.org/obo/DOID_0050739

subClassOf

http://purl.obolibrary.org/obo/DOID_0050739

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_0050736 BAO LOOM
http://purl.obolibrary.org/obo/DOID_0050736 BAO SAME_URI
http://purl.obolibrary.org/obo/DOID_0050736 DTO LOOM
http://purl.obolibrary.org/obo/DOID_0050736 DTO SAME_URI
http://purl.obolibrary.org/obo/DOID_0050736 MONDO SAME_URI
http://purl.obolibrary.org/obo/DOID_0050736 BAO LOOM
http://purl.obolibrary.org/obo/DOID_0050736 BAO SAME_URI
http://purl.obolibrary.org/obo/DOID_0050736 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0050736 NIFSTD SAME_URI
http://www.owl-ontologies.com/NPOntology.owl#DOID_0080002 NATPRO LOOM
http://purl.obolibrary.org/obo/MONDO_0000426 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0000426 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0000426 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0000426 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0000426 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0000426 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0000426 EFO LOOM