Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Simple ear |
Finding site |
False |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
orecchio da pipistrello |
Finding site |
False |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cat ear (disorder) |
Finding site |
False |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital absence of auricle with atresia of auditory canal |
Finding site |
False |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Ear auricle and external auditory canal absent |
Finding site |
False |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Polyotia |
Finding site |
False |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Polyotia |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital malposition of pinna |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital split ear lobe (disorder) |
Finding site |
False |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pinnal calcification (disorder) |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by aplasia cutis congenita of the scalp, breast anomalies ranging from hypothelia or athelia to amastia, and anomalies of the external ears. Variable clinical characteristics include nail and dental anomalies, syndactyly and camptodactyly of fingers and/or toes, sparse or absent secondary sexual hair, renal malformations, and facial dysmorphism. Cases with severe hypotonia and developmental delay have been reported. |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Temperature of pinna |
Inheres in |
False |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Intellectual disability-cataracts-calcified pinnae-myopathy syndrome is a rare, genetic intellectual disability syndrome characterized by macrocephaly, hypotonia, dysmorphic facial features (wide forehead, ptosis, downslanting palpebral fissures, enlarged and calcified external ears, large jaw), sparse body hair, tall stature, and intellectual disability. Hearing loss, insulin-resistant diabetes, and progressive distal muscle wasting (leading to joint contractures) have also been reported in adulthood. Rare manifestations include behavioral abnormalities (aggression and restlessness), hypothyroidism, cerebral calcification, ataxia, and peripheral neuropathy. |
Finding site |
False |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Numbness of pinna (finding) |
Finding site |
False |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Lop ear deformity |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Structure of left pinna |
Is a |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Structure of right pinna |
Is a |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Eminentia triangularis |
Is a |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital absence of auricle with stenosis of auditory canal |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Intellectual disability-cataracts-calcified pinnae-myopathy syndrome is a rare, genetic intellectual disability syndrome characterized by macrocephaly, hypotonia, dysmorphic facial features (wide forehead, ptosis, downslanting palpebral fissures, enlarged and calcified external ears, large jaw), sparse body hair, tall stature, and intellectual disability. Hearing loss, insulin-resistant diabetes, and progressive distal muscle wasting (leading to joint contractures) have also been reported in adulthood. Rare manifestations include behavioral abnormalities (aggression and restlessness), hypothyroidism, cerebral calcification, ataxia, and peripheral neuropathy. |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Ear auricle and external auditory canal absent |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital fistula of pinna of ear |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital cyst of pinna of ear |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute infection of pinna |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
On examination - ear auricle painful |
Finding site |
False |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pain in pinna |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital crumpled ear |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Structure of auricular muscle (body structure) |
Is a |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Infection of pierced pinna (disorder) |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Burn of pinna (disorder) |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Temperature of pinna |
Inheres in |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Malignant neoplasm of pinna |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Gouty tophus of pinna (disorder) |
Finding site |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Drainage of hematoma of pinna and insertion of bolster sutures |
Procedure site - Direct (attribute) |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Drainage of hematoma of pinna and insertion of bolster sutures |
Procedure site - Direct (attribute) |
True |
Pinna structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |