loading...| Preferred Name |
Horner Syndrome |
|
| Synonyms |
Horner Syndrome, Acquired |
|
| Definitions |
A syndrome associated with defective sympathetic innervation to one side of the face, including the eye. Clinical features include MIOSIS; mild BLEPHAROPTOSIS; and hemifacial ANHIDROSIS (decreased sweating)(see HYPOHIDROSIS). Lesions of the BRAIN STEM; cervical SPINAL CORD; first thoracic nerve root; apex of the LUNG; CAROTID ARTERY; CAVERNOUS SINUS; and apex of the ORBIT may cause this condition. (From Miller et al., Clinical Neuro-Ophthalmology, 4th ed, pp500-11) |
|
| ID |
http://purl.bioontology.org/ontology/MESH/D006732 |
|
| altLabel |
Horner Syndrome, Acquired Syndrome, Horner Syndrome, Bernard Ptosis Sympathetic Horners Syndrome Horners Syndrome, Pupil Syndrome, Bernard's Claude Bernard-Horner Syndrome Syndromes, Bernard Horner Syndrome, Central Sympathetic Ocular-Ophthalmoplegia Oculosympathetic Syndrome Bernards Syndrome Syndrome, Claude Bernard-Horner Ocular-Ophthalmoplegias, Sympathetic Syndrome, Pupil Horner's Bernard's Syndrome Sympathetic Ocular Ophthalmoplegia Claude Bernard Horner Syndrome Syndromes, Oculosympathetic Sympathetic Ocular-Ophthalmoplegias Ocular-Ophthalmoplegia, Sympathetic Central Horner Syndrome Acquired Horner Syndrome Ophthalmoplegias, Sympathetic Ocular Syndrome, Horner's Ophthalmoplegia, Sympathetic Ocular Syndrome, Oculosympathetic Horner's Syndrome Pupil Horner's Syndrome Bernard Syndromes Ocular Ophthalmoplegias, Sympathetic Horner's Syndrome, Pupil Syndrome, Central Horner Miosis, Innervational Defect Oculosympathetic Syndromes Sympathetic Ocular Ophthalmoplegias Ocular Ophthalmoplegia, Sympathetic Syndrome, Acquired Horner Bernard Syndrome Horner Syndrome, Pupil |
|
| AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
|
| cui |
C0751204 C0019937 C0751203 C0751205 C0338567 C0751206 |
|
| DC |
1 |
|
| definition |
A syndrome associated with defective sympathetic innervation to one side of the face, including the eye. Clinical features include MIOSIS; mild BLEPHAROPTOSIS; and hemifacial ANHIDROSIS (decreased sweating)(see HYPOHIDROSIS). Lesions of the BRAIN STEM; cervical SPINAL CORD; first thoracic nerve root; apex of the LUNG; CAROTID ARTERY; CAVERNOUS SINUS; and apex of the ORBIT may cause this condition. (From Miller et al., Clinical Neuro-Ophthalmology, 4th ed, pp500-11) |
|
| DX |
20000101 |
|
| HN |
2000(1966) |
|
| Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
|
| Machine permutation |
2000; see HORNER'S SYNDROME 1966-1999 |
|
| Mapped from | ||
| MDA |
19990101 |
|
| MMR |
20230405 |
|
| MN |
C23.888.592.708.362.500 C11.710.528.500 C10.597.690.362.500 C10.177.350 C10.228.140.232.750 |
|
| notation |
D006732 |
|
| prefLabel |
Horner Syndrome |
|
| TERMUI |
T365373 T365370 T365364 T365366 T365369 T373520 T020316 T365365 T020317 T365367 T365371 T365368 T365372 |
|
| TH |
NLM (2000) NLM (1966) NLM (1990) |
|
| tui |
T047 |
|
| subClassOf |
http://purl.bioontology.org/ontology/MESH/D001342 |