- ... Gravis, Neonatal C10.668.758.800 Myasthenic Syndromes, Congenital C10.668.829 Peripheral Nervous System Diseases C10.668.829.025 Acrodynia C10.668.829.050 Amyloid Neuropathies C10.668.829.050.050 Amyloid Neuropathies, Familial ...
- ... DISEASE TORTICOLLIS TREMOR NEUROLOGIC MANIFESTATIONS CONVULSIONS DELIRIUM DIABETIC NEUROPATHIES HALLUCINATIONS *HEMIANOPSIA MENINGISM REFLEX, ABNORMAL SENSATION DISORDERS (NON MESH) ANALGESIA, CONGENITAL HYPERESTHESIA HYPESTHESIA PARESTHESIA PHANTOM LIMB SPASM UNCONSCIOUSNESS COMA ...
- ... Hypoplasia Retinal Arterial Macroaneurysm Stargardt Disease Toxic Optic ... Failure Syndromes Shwachman-Diamond Syndrome 2020 ...
- ... Hypoplasia - Retinal Arterial Macroaneurysm - Stargardt Disease - Toxic Optic ... - Congenital Bone Marrow Failure Syndromes - Shwachman-Diamond Syndrome C16 ...
- ... following: o A significant abnormality on the ddC Neuropathy Targeted Symptom Questionnaire defined as a symptom score > ... drugs will be permanently discontinued for dose-limiting neuropathy defined as the occurrence of one of the ...
- ... the DNMT1 gene are associated with HEREDITARY SENSORY NEUROPATHY TYPE 1 class E. Tree locations: DNA (Cytosine- ... FAILURE; MULTIPLE MYELOMA; NEPHROTIC SYNDROME; RESTRICTIVE CARDIOMYOPATHY, and neuropathies. Tree locations: Amyloidosis C18.452.845.500.550 ...
- ... weak or paralyzed upper extremity. PI: Brachial Plexus Neuropathies (2000-2018) PI: Paralysis, Obstetric (1973-2018) PI: ... 614.131.294 C26.141.294 Brachial Plexus Neuropathies C10.668.829.100.750 Neuroglobin A vertebrate ...
- ... in C9 (OTORHINOLARYNGOLOGIC DISEASES). CATEGORY CIO & CATEGORY C16 NEUROPATHIES, HEREDITARY SENSORY AND AUTONOMIC (a new name) and NEUROPATHIES, HEREDITARY MOTOR AND SENSORY (a new heading) required ...
- ... 294 C26.141.294 Parent Heading: Brachial Plexus Neuropathies C10.668.829.100.750 C16.614.131. ... severe pain, and of pain associated with DIABETIC NEUROPATHIES. Parent Heading: Phenols D02.455.426.559.389. ...
- ... 800.575.912.250.100.906 Toxic Optic Neuropathy Damage to the eye or its function (e. ... Attributes C23.550.291.968 Univentricular Heart Rare congenital heart malformation with a single ventricle (HEART VENTRICLES) ...
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