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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.550 Joint Diseases .
C05.550.629 Nail-Patella Syndrome .
C10 Nervous System Diseases .
C10.177 Autonomic Nervous System Diseases .
C10.177.350 Horner Syndrome .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.546 Headache Disorders .
C10.228.140.546.399 Headache Disorders, Primary .
C10.228.140.546.399.937 Trigeminal Autonomic Cephalalgias .
C10.228.140.546.399.937.500 Cluster Headache .
C10.597 Neurologic Manifestations .
C10.597.690 Pupil Disorders .
C10.597.690.362 Miosis .
C10.597.690.362.500 Horner Syndrome .
C11 Eye Diseases .
C11.710 Pupil Disorders .
C11.710.528 Miosis .
C11.710.528.500 Horner Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.606 Nail-Patella Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.600 Nail-Patella Syndrome .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.529 Nail Diseases .
C17.800.529.400 Nail-Patella Syndrome .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.708 Pupil Disorders .
C23.888.592.708.362 Miosis .
C23.888.592.708.362.500 Horner Syndrome .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Nail-Patella Syndrome .
Fong Disease .
Hereditary Onycho-Osteodysplasia .
Hereditary Osteo-Onychodysplasias .
Onychoosteodysplasia .
Disease, Fong .
Hereditary Osteo-Onychodysplasia .
Nail Patella Syndrome .
Osteo Onychodysplasia, Hereditary .
Osteo-Onychodysplasias, Hereditary .
Syndrome, Nail-Patella .
Syndrome, Osterreicher .
Syndrome, Pelvic Horn .
Syndrome, Turner-Kieser .
Turner Kieser Syndrome .
Osteo-Onychodysplasia, Hereditary .
Osterreicher Syndrome .
Pelvic Horn Syndrome .
Turner-Kieser Syndrome .
A syndrome of multiple abnormalities characterized by the absence or hypoplasia of the PATELLA and congenital nail dystrophy. It is a genetically determined autosomal dominant trait. .
1.00
 
Horner Syndrome .
Bernard's Syndrome .
Claude Bernard-Horner Syndrome .
Horner Syndrome, Acquired .
Horner Syndrome, Central .
Horner's Syndrome, Pupil .
Ophthalmoplegia, Sympathetic Ocular .
Ptosis Sympathetic .
Sympathetic Ocular-Ophthalmoplegia .
Acquired Horner Syndrome .
Bernard Syndromes .
Bernards Syndrome .
Central Horner Syndrome .
Claude Bernard Horner Syndrome .
Horner Syndrome, Pupil .
Horners Syndrome .
Horners Syndrome, Pupil .
Ocular Ophthalmoplegia, Sympathetic .
Ocular Ophthalmoplegias, Sympathetic .
Ocular-Ophthalmoplegia, Sympathetic .
Ocular-Ophthalmoplegias, Sympathetic .
Oculosympathetic Syndromes .
Ophthalmoplegias, Sympathetic Ocular .
Pupil Horner's Syndrome .
Sympathetic Ocular Ophthalmoplegia .
Sympathetic Ocular Ophthalmoplegias .
Sympathetic Ocular-Ophthalmoplegias .
Syndrome, Acquired Horner .
Syndrome, Bernard .
Syndrome, Bernard's .
Syndrome, Central Horner .
Syndrome, Claude Bernard-Horner .
Syndrome, Horner .
Syndrome, Horner's .
Syndrome, Oculosympathetic .
Syndrome, Pupil Horner's .
Syndromes, Bernard .
Syndromes, Oculosympathetic .
Bernard Syndrome .
Horner's Syndrome .
Miosis, Innervational Defect .
Oculosympathetic Syndrome .
BERNARD'S SYNDROME .
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) .
0.64
441694
 
Cluster Headache .
Atypical Cluster Headache .
Chronic Cluster Headache .
Cluster Headache Syndrome .
Episodic Cluster Headache .
Horton's Syndrome .
Atypical Cluster Headaches .
Cephalgia, Histamine .
Cephalgias, Histamine .
Chronic Cluster Headaches .
Ciliary Neuralgias .
Cluster Headache Syndromes .
Cluster Headache, Atypical .
Cluster Headache, Chronic .
Cluster Headache, Episodic .
Cluster Headaches .
Cluster Headaches, Atypical .
Cluster Headaches, Chronic .
Cluster Headaches, Episodic .
Episodic Cluster Headaches .
Headache Syndrome, Cluster .
Headache Syndromes, Cluster .
Headache, Atypical Cluster .
Headache, Chronic Cluster .
Headache, Episodic Cluster .
Headaches, Atypical Cluster .
Headaches, Chronic Cluster .
Headaches, Cluster .
Headaches, Episodic Cluster .
Histamine Cephalgias .
Hortons Syndrome .
Migraine, Neuralgic .
Migraines, Neuralgic .
Neuralgia, Ciliary .
Neuralgias, Ciliary .
Neuralgic Migraines .
Syndrome, Cluster Headache .
Syndrome, Horton .
Syndrome, Horton's .
Syndromes, Cluster Headache .
Ciliary Neuralgia .
Headache, Cluster .
Histamine Cephalgia .
Horton Syndrome .
Neuralgic Migraine .
A primary headache disorder that is characterized by severe, strictly unilateral PAIN which is orbital, supraorbital, temporal or in any combination of these sites, lasting 15-180 min. occurring 1 to 8 times a day. The attacks are associated with one or more of the following, all of which are ipsilateral: conjunctival injection, lacrimation, nasal congestion, rhinorrhea, facial SWEATING, eyelid EDEMA, and miosis. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) .
0.58
362344