WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0090108 autosomal dominant hypocalcemia 2 Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  An autosomal dominant hypocalcemia that has_material_basis_in heterozygous mutation in the G protein subunit alpha 11 gene (GNA11) on chromosome 19p13.

1 Ontology

Name
Disease Ontology

10 Parents

Identifier Name Description
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:0014667 disease of metabolism A disease that involves errors in metabolic processes of building or degradation of molecules.
DOID:0050177 monogenic disease A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive.
DOID:630 genetic disease A disease that has_material_basis_in genetic variations in the human genome.
DOID:0050736 autosomal dominant disease 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.
DOID:0050739 autosomal genetic disease A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes.
DOID:655 inherited metabolic disorder A disease of metabolism that is characterized by enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to inherited enzyme abnormality.
DOID:896 metal metabolism disorder An inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals.
DOID:0090109 autosomal dominant hypocalcemia A metal metabolism disorder characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone.
DOID:0090108 autosomal dominant hypocalcemia 2 An autosomal dominant hypocalcemia that has_material_basis_in heterozygous mutation in the G protein subunit alpha 11 gene (GNA11) on chromosome 19p13.

9 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0090109 DOID:0090108
is_a DOID:655 DOID:0090108
is_a DOID:0050177 DOID:0090108
is_a DOID:0050739 DOID:0090108
is_a DOID:896 DOID:0090108
is_a DOID:0050736 DOID:0090108
is_a DOID:630 DOID:0090108
is_a DOID:0014667 DOID:0090108
is_a DOID:4 DOID:0090108

1 Synonyms

Name Type
HYPOC2 synonym