WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0111576 dehydrated hereditary stomatocytosis 1 Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A dehydrated hereditary stomatocytosis that has_material_basis_in heterozygous mutation in the PIEZO1 gene on chromosome 16q24.3.

1 Ontology

Name
Disease Ontology

12 Parents

Identifier Name Description
DOID:7 disease of anatomical entity A disease that manifests in a defined anatomical structure.
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: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:74 hematopoietic system disease A disease of anatomical entity that has_material_basis_in hematopoietic cells.
DOID:2355 anemia A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells.
DOID:583 hemolytic anemia A normocytic anemia that is characterized by the rate of descruction of red blood cells exceeding the rate than they can be made.
DOID:720 normocytic anemia An anemia that is characterized by circulating red blood cells that are the same size and have a normal red color and a mean corpuscular volume (MCV) between 80 and 100 fL.
DOID:0111575 dehydrated hereditary stomatocytosis A hemolytic anemia characterized by altered intracellular cation content and cellular dehydration of erythocytes resulting in increased mean corpuscular hemoglobin concentrations and altered cell shapes.
DOID:0111576 dehydrated hereditary stomatocytosis 1 A dehydrated hereditary stomatocytosis that has_material_basis_in heterozygous mutation in the PIEZO1 gene on chromosome 16q24.3.

11 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0050736 DOID:0111576
is_a DOID:0111575 DOID:0111576
is_a DOID:2355 DOID:0111576
is_a DOID:0050739 DOID:0111576
is_a DOID:583 DOID:0111576
is_a DOID:630 DOID:0111576
is_a DOID:7 DOID:0111576
is_a DOID:720 DOID:0111576
is_a DOID:0050177 DOID:0111576
is_a DOID:4 DOID:0111576
is_a DOID:74 DOID:0111576

4 Synonyms

Name Type
dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema synonym
pseudohyperkalemia edinburgh synonym
pseudohyperkalemia familial 1, due to red cell leak synonym
PSHK1 synonym