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 |