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45486003: Aplasia (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
75833016 Aplasia en Synonym Active Entire term case insensitive SNOMED CT core module
75834010 Aplasia, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
782730017 Aplasia (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Aplasia Is a Maturation defect true Inferred relationship Existential restriction modifier
Aplasia Is a Developmental anomaly false Inferred relationship Existential restriction modifier
Aplasia Is a Absence true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Hydranencephaly Associated morphology False Aplasia Inferred relationship Existential restriction modifier 2
Pulmonary valve agenesis, tetralogy of Fallot, absence of ductus arteriosus syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 3
Aniridia, renal agenesis, psychomotor retardation syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome Associated morphology False Aplasia Inferred relationship Existential restriction modifier 3
Partial agenesis of corpus callosum Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
Hemicephaly Associated morphology False Aplasia Inferred relationship Existential restriction modifier 2
Curry Jones syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 3
Hydranencephaly with proliferative vasculopathy Associated morphology False Aplasia Inferred relationship Existential restriction modifier 2
Congenital absence of part of brain Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
Congenital tibial deficiency type II Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia of uterine cervix Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia of body of uterus Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Hereditary isolated aplastic anemia Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Absent thumb with short stature and immunodeficiency syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Mullerian aplasia Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
WNT4 Müllerian aplasia and ovarian dysfunction Associated morphology True Aplasia Inferred relationship Existential restriction modifier 2
Ablepharon of bilateral eyelids Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
Ablepharon of bilateral eyelids Associated morphology False Aplasia Inferred relationship Existential restriction modifier 2
Congenital absence of seminal vesicle Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Transverse deficiency Is a True Aplasia Inferred relationship Existential restriction modifier
Autosomal dominant Robinow syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 4
Autosomal recessive Robinow syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 4
B cell lymphocyte aplasia caused by drug Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Congenital absence of skin on scalp with epidermal nevi Associated morphology True Aplasia Inferred relationship Existential restriction modifier 2
Totally absent pericardium Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Congenital absence of germinal epithelium of testes Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Adams-Oliver syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Congenital absence of skin on scalp Associated morphology True Aplasia Inferred relationship Existential restriction modifier 2
Aplasia cutis congenita due to underlying malformation (Type 4) Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita associated with fetus papyraceus (Type 5) Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita due to teratogenic drug (Type 7) Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita following intra-uterine infection (Type 8) Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Oculocerebrocutaneous syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis in Trisomy 13 syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis in Johanson-Blizzard syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis with myopia syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita with intestinal lymphangiectasia syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 2
Aplasia cutis congenita with epibulbar dermoid syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 2
Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome Associated morphology True Aplasia Inferred relationship Existential restriction modifier 2
Didymosis aplasticosebacea Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita of limb Associated morphology True Aplasia Inferred relationship Existential restriction modifier 2
Autosomal recessive aplasia cutis congenita of limb Associated morphology True Aplasia Inferred relationship Existential restriction modifier 2
Partial absence of septum pellucidum Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Congenital partial absence of gastric muscle Associated morphology True Aplasia Inferred relationship Existential restriction modifier 1
Transient acquired pure red cell aplasia Associated morphology True Aplasia Inferred relationship Existential restriction modifier 4
[X]Other specified aplastic anaemias Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
[X]Other acquired pure red cell aplasias Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
[X]Acquired pure red cell aplasia, unspecified Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
Aplastic anemia NOS (disorder) Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
Constitutional aplastic anemia without mention of malformation (disorder) Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
Acquired aplastic anemia NOS (disorder) Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
Other specified constitutional aplastic anemia (disorder) Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
Secondary red cell aplasia NEC Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
Constitutional aplastic anemia NOS (disorder) Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1
Erythropoiesis stimulating agent induced antibody mediated acquired pure red cell aplasia Associated morphology False Aplasia Inferred relationship Existential restriction modifier 1

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