WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0060699 familial hypocalciuric hypercalcemia Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A hypercalcemia characterized by autosomal dominant inheritance with elevation of serum calcium levels and decreased urinary calcium excretion.

1 Ontology

Name
Disease Ontology

12 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:0060158 acquired metabolic disease A disease of metabolism that has_material_basis_in enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to an endocrine organ disease, organ malfunction, inadequate intake, dietary deficiency, or malabsorption.
DOID:0050032 mineral metabolism disease An acquired metabolic disease that is characterized by abnormal mineral metabolism.
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:0060699 familial hypocalciuric hypercalcemia A hypercalcemia characterized by autosomal dominant inheritance with elevation of serum calcium levels and decreased urinary calcium excretion.
DOID:12678 hypercalcemia  
DOID:10575 calcium metabolism disease  

14 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0050736 DOID:0060699
is_a DOID:12678 DOID:0060699
is_a DOID:655 DOID:0060699
is_a DOID:0050032 DOID:0060699
is_a DOID:0060158 DOID:0060699
is_a DOID:0050177 DOID:0060699
is_a DOID:10575 DOID:0060699
is_a DOID:0050739 DOID:0060699
is_a DOID:630 DOID:0060699
is_a DOID:0014667 DOID:0060699
is_a DOID:4 DOID:0060699
is_a DOID:0060699 DOID:0060700
is_a DOID:0060699 DOID:0060701
is_a DOID:0060699 DOID:0060702

5 Synonyms

Name Type
FBH synonym
FBHH synonym
FHH synonym
familial benign hypercalcemia synonym
familial benign hypocalciuric hypercalcemia synonym