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25659002: Narrowed structure (morphologic abnormality)


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

Descriptions:

Id Description Lang Type Status Case? Module
756001013 Narrowed structure (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2770179010 Narrowed structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
43009019 Narrowing en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
756001013 Narrowed structure (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
756001013 Narrowed structure (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2770179010 Narrowed structure en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2770179010 Narrowed structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
12851000077114 rétrécissement fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
12851000077114 rétrécissement fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


10 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Narrowed structure (morphologic abnormality) Is a Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept)
Narrowed structure (morphologic abnormality) Is a Mechanical lesion true Inferred relationship Existential restriction modifier (core metadata concept)
Narrowed structure (morphologic abnormality) Is a Narrowing (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Pulmonary emphysema in alpha-1 PI deficiency Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Toxic emphysema Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Scar emphysema Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Segmental bullous emphysema Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Other specified perinatal interstitial emphysema or related condition Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chronic obstructive pulmonary disease Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Acute infective exacerbation of chronic obstructive pulmonary disease Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Pulmonary emphysema (disorder) Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Chronic bullous emphysema Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Hemolytic anemia with emphysema AND cutis laxa (disorder) Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chronic diffuse emphysema caused by inhalation of chemical fumes AND/OR vapors Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Senile blepharophimosis Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chronic obstructive airways disease NOS Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Cicatricial blepharophimosis Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Acute exacerbation of chronic obstructive airways disease Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Spastic blepharophimosis Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Other specified chronic obstructive airways disease Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Vanishing lung Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chronic obstructive pulmonary disease with acute lower respiratory infection (disorder) Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blepharophimosis Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Acquired blepharophimosis Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Blepharophimosis syndrome Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
[X]Other specified chronic obstructive pulmonary disease Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Unilateral emphysema Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Narrow gingival width Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Repair of blepharophimosis Direct morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Obstructive emphysema Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Compensatory emphysema Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chronic obstructive pulmonary disease with acute exacerbation, unspecified Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital lobar emphysema (disorder) Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Bronchial atresia with segmental pulmonary emphysema (disorder) Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Cystic-bullous disease of the lung Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe chronic obstructive pulmonary disease Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Giant bullous emphysema Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Panacinar emphysema (disorder) Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Interstitial emphysema of lung Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Narrowing of intervertebral disc space Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Perinatal interstitial emphysema or related condition NOS Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Anatomical narrow angle glaucoma with borderline intraocular pressure (disorder) Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Anatomical narrow angle glaucoma with borderline intraocular pressure (disorder) Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Narrowing or closure of fetal ductus arteriosus Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Narrowing of fetal ductus arteriosus (disorder) Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Chronic obstructive airway disease with asthma Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Acute exacerbation of chronic obstructive pulmonary disease with asthma Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Ohdo syndrome, Maat-Kievit-Brunner type Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 5
Rare syndrome with the association of congenital hypothyroidism, facial dysmorphism (microcephaly, blepharophimosis, a bulbous nose, thin lip, low-set ears and micrognathia), postaxial polydactyly and severe intellectual deficit. Cryptorchidism is present in affected males. Some patients also have cardiac anomalies (interventricular communication), hypotonia and growth delay. Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 5
Congenital blepharophimosis of upper eyelid Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital blepharophimosis of lower eyelid Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital blepharophimosis of lower eyelid Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Mental retardation, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Blepharophimosis syndrome Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blepharophimosis Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Ohdo syndrome, Maat-Kievit-Brunner type Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital blepharophimosis of upper eyelid Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Rare syndrome with the association of congenital hypothyroidism, facial dysmorphism (microcephaly, blepharophimosis, a bulbous nose, thin lip, low-set ears and micrognathia), postaxial polydactyly and severe intellectual deficit. Cryptorchidism is present in affected males. Some patients also have cardiac anomalies (interventricular communication), hypotonia and growth delay. Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Blepharophimosis syndrome Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 4
Blepharophimosis epicanthus inversus ptosis syndrome Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare syndrome characterised by the association of blepharophimosis and ptosis, V-esotropia, and weakness of extraocular and frontal muscles with syndactyly of the toes, short stature, prognathism, and hypertrophy and fusion of the eyebrows. Associated morphology False Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 4
A rare syndrome characterised by the association of blepharophimosis and ptosis, V-esotropia, and weakness of extraocular and frontal muscles with syndactyly of the toes, short stature, prognathism, and hypertrophy and fusion of the eyebrows. Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Small left colon syndrome Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Blepharophimosis, intellectual disability syndrome, Verloes type (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Coarctation Is a True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Blepharophimosis, intellectual disability syndrome (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Narrowing of fetal ductus arteriosus (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired blepharophimosis of bilateral eyelids (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired blepharophimosis of bilateral eyelids (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital blepharophimosis of bilateral eyelids (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blepharophimosis of bilateral eyelids (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Blepharophimosis epicanthus inversus ptosis syndrome plus (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Blepharophimosis epicanthus inversus ptosis syndrome Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired blepharophimosis of left palpebral fissure (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired blepharophimosis of right palpebral fissure (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blepharophimosis of left palpebral fissure (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital blepharophimosis of right palpebral fissure Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2-related blepharophimosis, intellectual disability syndrome (disorder) Associated morphology True Narrowed structure (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1

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