Related by context. All words. (Click for frequent words.) 66 optic nerve hypoplasia 65 Crouzon syndrome 65 optic atrophy 64 aniridia 63 brain malformation 63 retinal dysfunction 63 cortical blindness 63 congenital cataract 62 spastic diplegia 62 discoid lupus 62 congenital cataracts 62 microtia 62 ectodermal dysplasia 61 congenital muscular dystrophy 61 Usher Syndrome 61 Hurler syndrome 61 congenital glaucoma 61 sensorineural hearing loss 60 cardio myopathy 60 hereditary spastic paraplegia 60 retinal blastoma 60 Proteus syndrome 60 Leber congenital amaurosis LCA 60 Neurofibromatosis type 60 CHARGE syndrome 60 Chiari malformation 60 Ehlers Danlos syndrome 60 pigmentosa 60 fibrous dysplasia 60 retinitis pigmentosa RP 60 muscular degeneration 59 macular disease 59 globus 59 Hutchinson Gilford progeria 59 skeletal dysplasia 59 arthrogryposis multiplex congenita 59 autosomal dominant polycystic kidney 59 recessive genetic 59 Goldenhar Syndrome 59 neurogenetic 59 cortical dysplasia 59 static encephalopathy 59 Leber congenital amaurosis 59 Henoch purpura 59 congential 59 hydrops 59 Raynaud disease 59 verbal apraxia 58 rare chromosomal disorder 58 nonhereditary 58 ischemic optic neuropathy 58 proliferative retinopathy 58 Apert syndrome 58 glaucoma cataract 58 celebral palsy 58 dysphasia 58 Hip dysplasia 58 Erb palsy 58 optic neuritis 58 chiari malformation 58 osteopetrosis 58 Barrett esophagus precancerous 58 neurocysticercosis 58 facial palsy 58 clubfeet 58 congenital insensitivity 58 prematurity ROP 58 dominantly inherited 58 Pelizaeus Merzbacher disease 58 Perthes disease 58 Retinitis Pigmentosa RP 58 severely impairs 58 spastic cerebral palsy 58 Bacterial vaginosis 58 Hirschsprung Disease 57 spastic paraplegia 57 retinitis 57 Joubert syndrome 57 retinal hemorrhage 57 myelopathy 57 arthrogryposis 57 benign positional vertigo 57 TMJ disorder 57 septo optic dysplasia 57 Retinoblastoma 57 medium chain acyl 57 osteogenesis imperfecta 57 disorder thalassemia 57 Hypertrophic 57 undiagnosed celiac disease 57 Cockayne syndrome 57 atresia 57 retinitis pigmentosa degenerative 57 neurodermatitis 57 Langerhans cell histiocytosis 57 congenital diaphragmatic hernia 57 Von Willebrand disease 57 multiorgan 57 Alport syndrome 57 myoclonic epilepsy 57 infantile hemangioma 57 degenerative retinal disease 57 mitochondrial myopathy 57 muscular atrophy 57 vascular birthmarks 57 esophageal reflux 57 paresis 56 arachnoiditis 56 adenomyosis 56 Myasthenia gravis 56 neurologic deficits 56 corneal edema 56 systemic scleroderma 56 leukoencephalopathy 56 Wilms tumors 56 Dysplasia 56 embryonal rhabdomyosarcoma 56 BH4 deficiency 56 irreversible blindness 56 bilateral retinoblastoma 56 migraine aura 56 neurologic disorder 56 Leber Congenital Amaurosis LCA 56 Diabetic neuropathy 56 inherited retinal 56 fibroma 56 Stargardt Macular Dystrophy 56 otitis 56 torticollis 56 idiopathic pulmonary 56 Churg Strauss syndrome 56 expressive aphasia 56 Morquio syndrome 56 Irlen Syndrome 56 holoprosencephaly 56 juvenile dermatomyositis 56 hypertrophic cardiomyopathy HCM 56 neurosensory 56 plexiform 56 Sjögren syndrome 56 polycystic kidneys 56 Down syndrome chromosomal disorder 56 congenital disorder 56 Asperger Disorder 56 Benign Paroxysmal Positional Vertigo 56 achromatopsia 56 spondylolysis 56 Crouzon Syndrome 56 profound deafness 56 benign paroxysmal positional vertigo 56 congenital scoliosis 56 cerebellar hypoplasia 56 pseudotumor cerebri 56 thyroid deficiency 56 photosensitivity 56 Nasal allergies 56 Angelman syndrome 56 achondroplasia 56 hemiparesis 56 infantile hemangiomas 56 congenita 56 chronic autoimmune disorder 56 microvascular dysfunction 56 pulmonary stenosis 56 autosomal dominant inheritance 56 hereditary deafness 56 oro facial 56 hereditary degenerative 56 optic neuropathy 55 optic nerve atrophy 55 dyskeratosis congenita 55 chromosome abnormality 55 corneal scarring 55 thoracic aortic aneurysm 55 polymyalgia rheumatica 55 diffuse intrinsic pontine glioma 55 congenital blindness 55 dysautonomia 55 impaired cognition 55 choroidal vasculopathy 55 autosomal dominant disorder 55 de novo mutations 55 Aicardi syndrome 55 iritis 55 acute psychosis 55 neuro developmental disorder 55 synaesthesia 55 PCNSL 55 neuritis 55 Myotonic dystrophy 55 amblyopic 55 otosclerosis 55 lipodystrophy syndrome 55 Noonan Syndrome 55 hypothalamic hamartoma 55 Chiari Malformation 55 cholestasis 55 dysphonia 55 Brugada syndrome 55 Brugada Syndrome 55 esophageal atresia 55 multisystem disease 55 cleft lip palate 55 ischemic vascular 55 Charcot foot 55 radiculopathy 55 auditory neuropathy 55 incurable neurodegenerative disease 55 lactase deficiency 55 xeroderma pigmentosum 55 dysgenesis 55 ADPKD 55 Meniere Disease 55 valvular heart disease 55 Treacher Collins syndrome 55 VCFS 55 Myelodysplastic syndrome 55 primary hyperoxaluria 55 hypotonia 55 POAG 55 savant syndrome 55 apraxia 55 cystic kidney 55 rheumatic disease 55 cutaneous lupus 55 gene MECP2 55 osteochondrosis 55 autoimmune thyroiditis 55 G6PD deficiency 55 degenerative neurological disorder 55 superior mesenteric artery 55 Raynaud syndrome 55 paraneoplastic 55 Sanfilippo Syndrome 55 imperfecta 55 Hirschsprung disease 55 congenital disorders 55 leukodystrophy 55 Severe Primary IGFD 55 cranio 54 polymyalgia 54 retinoblastoma rare 54 venous malformation 54 thyroid dysfunction 54 esotropia 54 prosopagnosia 54 neonatal respiratory distress 54 LHON 54 chronic venous insufficiency 54 DiGeorge Syndrome 54 degenerative disorder 54 Leber Congenital Amaurosis 54 glomerulonephritis 54 cerebellar ataxia 54 alpha1 antitrypsin deficiency 54 temporoparietal 54 recessive trait 54 proliferative diabetic retinopathy 54 juvenile myelomonocytic leukemia 54 obstructive sleep 54 pituitary adenoma 54 idiopathic epilepsy 54 incurable genetic 54 brachial plexus palsy 54 spontaneous remission 54 Moyamoya 54 temporomandibular joint disorder 54 anterior ischemic optic neuropathy 54 ADA SCID 54 exertional headaches 54 mycosis 54 Alport Syndrome 54 neuropsychiatric disorder 54 diffuse axonal injury 54 Treacher Collins Syndrome 54 fibromatosis 54 neuropsychological impairments 54 myasthenia gravis neuromuscular 54 corneal opacity 54 Acanthamoeba infections 54 cervical spondylosis 54 Krabbe Leukodystrophy 54 incurable neurological disorder 54 idiopathic PAH 54 chromosomal disorder 54 systemic amyloidosis 54 Retinopathy 54 lysosomal storage diseases 54 primitive neuroectodermal tumors 54 Osteogenesis imperfecta 54 autistic tendencies 54 Leber Hereditary Optic Neuropathy 54 detached retinas 54 myalgic encephalomyelitis ME 54 lissencephaly 54 craniofacial deformities 54 carcinoid tumor 54 Eisenmenger syndrome 54 antiphospholipid syndrome 54 Porphyria 54 dissecans 54 giant cell arteritis 54 Moebius syndrome 54 paralysis blindness 54 malabsorption syndrome 54 urolithiasis 54 corneal diseases 54 bulbar 54 neurofibroma 54 spasmodic dysphonia 54 sarcoid 54 inherited retinal degeneration 54 renal agenesis 54 Crohns disease 54 retinal vascular 54 TMJD 54 paranasal sinus 54 nasal obstruction 54 neovascular glaucoma 54 pulmonary hypertension PH 54 congenital deafness 54 Dravet syndrome 54 corneal ectasia 54 quadriplegic cerebral palsy 54 cataract glaucoma 54 oculomotor 54 Hurler Syndrome 54 hemiplegia 54 Goldenhar syndrome 54 ocular inflammatory 54 chronic urticaria 54 corneal dystrophy 54 Cleft palate 54 diabetic retinopathy DR 54 Atopic dermatitis 54 Genetic predisposition 54 Leber hereditary optic neuropathy 54 WAGR syndrome 54 Dr. Gozal 54 ANCA associated 54 orofacial 54 hippocampal sclerosis 54 hereditary hemorrhagic telangiectasia 53 cervical vertigo 53 Iron deficiency anemia 53 chronic sinus infections 53 ovarian malignancy 53 cataracts glaucoma 53 Sturge Weber syndrome 53 neurological disorder affecting 53 arthropathy 53 orthostatic intolerance 53 cataracts 53 truncus arteriosus 53 congenital hypothyroidism 53 Gender Identity Disorder GID 53 nerve palsy 53 Rett syndrome neurological disorder 53 polycystic 53 hypertensive retinopathy 53 nonarteritic anterior ischemic optic 53 progressive retinal degenerative 53 autonomic dysfunction 53 Tourette syndrome neurological disorder 53 abdominal abscesses 53 cleft palette 53 neurogenic bladder 53 neuro degenerative disorder 53 situs inversus 53 hemolytic 53 thyroiditis 53 Congenital Muscular Dystrophy 53 Arnold Chiari Malformation 53 hyperstimulation 53 retinitis pigmentosa hereditary 53 Beta thalassemia 53 neurocognitive dysfunction 53 degenerative spinal 53 retinal detachment 53 DIPG 53 Bells Palsy 53 sympathetic ophthalmia 53 neuroblastoma tumor 53 retinal dystrophy 53 meningeal 53 WDR# 53 retinal degenerative disease 53 underlying pathophysiology 53 glaucoma macular degeneration 53 MCAD deficiency 53 Magnesium deficiency 53 nonalcoholic cirrhosis 53 tricuspid atresia 53 kidney insufficiency 53 Keratoconus 53 congenital 53 diabetes insipidus 53 retinal haemorrhage 53 streptococcus infection 53 Vitamin B# deficiency 53 congenital deficiency 53 haemolytic anemia 53 thyroid hormone deficiency 53 multi infarct dementia 53 Zinc deficiency 53 Niemann Pick disease 53 depersonalization disorder 53 lymphangioleiomyomatosis LAM 53 CdLS 53 myopathies 53 cyanotic 53 syringomyelia 53 GBA mutations 53 pulmonary atresia 53 dysfunctional voiding 53 interstitial nephritis 53 neurofibromas 53 familial hypercholesterolaemia FH 53 orofacial pain 53 cerebral palsy epilepsy 53 autism neurological disorder 53 skeletal fluorosis 53 osteogenesis imperfecta OI 53 Bi Polar Disorder 53 comorbid anxiety 53 Fuchs dystrophy 53 degenerative neurological diseases 53 epigastric pain 53 optic neuropathy NAION 53 neuropathies 53 degenerative retinal diseases 53 radiographic findings 53 Polycythemia 53 cardiomyopathy weakening 53 dystrophies 53 sequela 53 velo cardio facial 53 Chronic pancreatitis 53 PPCM 53 PCOD 53 microangiopathy 53 keratoconus 53 intractable epilepsy 53 collagen crosslinking 53 neuro muscular 53 LVNC 53 neurodevelopment disorder 53 alzheimer disease 53 chronic granulomatous disease 53 Apert Syndrome 53 blood clotting disorder 53 myopia nearsightedness 53 neurological 53 Irritable bowel syndrome 53 molar pregnancy 53 congenital anomaly 53 hyperreflexia 53 upper airway obstruction 53 petit mal seizures 53 immunodeficiency disorder 53 Uveal melanoma 53 entropion 53 immunodeficiencies 53 Raynaud phenomenon 53 nasal endoscopy 53 immuno deficiency 53 Critical limb ischemia 53 adrenal hyperplasia 53 lichen planus 53 subsyndromal 53 Pervasive Developmental Disorder 53 Capgras 53 Retinitis pigmentosa 53 bullous 53 moyamoya 52 aortic root aneurysm 52 somatoform disorder 52 Crigler Najjar syndrome 52 hypertrichosis 52 neurological manifestations 52 arthrosis 52 reproductive endocrine 52 temporal arteritis 52 edema swelling 52 autosomal recessive genetic 52 Mitochondrial disease 52 Parkinsons disease 52 autoimmune encephalitis 52 herpetic 52 Hashimoto thyroiditis 52 supratentorial 52 Parkinson disease degenerative 52 retinal detachments 52 Becker muscular dystrophy 52 Wegener granulomatosis 52 femoroacetabular impingement 52 anterior temporal 52 Degenerative disc disease 52 sensory disturbances 52 cardiac insufficiency 52 neuro developmental 52 Sjogren Syndrome 52 primary ciliary dyskinesia 52 adrenal function 52 anhidrosis 52 akinetic mutism 52 hemophagocytic lymphohistiocytosis 52 enterocolitis 52 neurobiological disorder 52 neurofibromatosis 52 biliary obstruction 52 vestibular dysfunction 52 Heavy menstrual bleeding 52 Legg Calvé Perthes disease 52 Peutz Jeghers syndrome 52 bone deformities 52 vascular anomalies 52 Nephrogenic Systemic Fibrosis NSF 52 Wernicke Korsakoff syndrome 52 atrioventricular septal defect 52 diaphragmatic hernia 52 macular 52 Congenital Adrenal Hyperplasia 52 gastroduodenal 52 inherited mutations 52 drooping eyelid 52 retinal haemorrhages 52 Pulmonary fibrosis 52 hippocampal function 52 craniosynostosis 52 glare halos 52 urinary blockage 52 ulnar neuropathy 52 Pompe Disease 52 neovascularisation 52 degenerative neurological disease 52 debilitating neurological disease 52 levodopa induced 52 enteropathy 52 SIADH 52 atrophic 52 vascular dysfunction 52 pulmonary hypoplasia 52 Wilms Tumor 52 progressive neurodegenerative 52 familial adenomatous polyposis 52 Lactose intolerance 52 retina macula 52 neuro degenerative disorders 52 myotonic dystrophy 52 polycystic kidney 52 respiratory gastrointestinal 52 Optic nerve 52 alveolar rhabdomyosarcoma 52 deformational plagiocephaly 52 cardiac fibrosis 52 Retinal vein occlusion 52 Diamond Blackfan Anemia 52 hamartoma 52 Osteogenesis Imperfecta 52 nonalcoholic steatohepatitis NASH 52 Prognostic factors 52 Parkinsons Disease 52 primary pulmonary hypertension 52 pulmonary infiltrates 52 Histiocytosis 52 neurodevelopmental disorder 52 corneal ulcer 52 degenerative neurological 52 sub syndromal 52 renal kidney 52 galactosemia 52 BPPV 52 NF2 52 pyelonephritis 52 Tourette Syndrome neurological disorder 52 pyloric stenosis 52 primary aldosteronism 52 induced cardiomyopathy 52 nonischemic 52 myofascial pain syndrome 52 intracerebral haemorrhage 52 radicular 52 spastic quadriplegia 52 smoldering myeloma 52 dysgraphia 52 neovascular 52 Nonspecific 52 biochemical abnormalities 52 agenesis 52 osteogenic sarcoma 52 exudative 52 gastrointestinal dysfunction 52 syncopal episode 52 neurocognitive deficits 52 Wernicke encephalopathy 52 clefting 52 eosinophilic 52 atypical hemolytic uremic syndrome 52 type 1diabetes 52 ataxias 52 hemorrhagic pancreatitis 52 amnestic 52 acidemia 52 polyhydramnios 52 histiocytosis 52 intracranial hypertension 52 gait disturbance 52 glaucoma cataracts 52 neurological dysfunctions 52 vasovagal syncope 52 perinatal asphyxia 52 Urticaria 52 interstitial pneumonia 52 Ventricular Septal Defect 52 reflux disease 52 spinal bifida 52 primary hyperparathyroidism 52 Smith Magenis syndrome 52 Sturge Weber Syndrome 52 pediatric cataract 52 parkinsonism 52 cardiac tamponade 52 pathophysiologic 52 Lafora disease 52 alkalosis 52 optica 52 Stargardt Disease 52 angioma 52 bronchopulmonary dysplasia BPD 52 Macular degeneration 52 clotting disorder 52 plexiform neurofibromas 52 disc degeneration 52 Angelman Syndrome 52 AAT deficiency 52 progressive neuromuscular 52 deficiency syndrome 52 vocal cord paresis 52 tetraplegia 52 Beckwith Wiedemann Syndrome 52 presbyopic 52 dermopathy 52 Nicotine dependence 52 airway obstructions 52 epidermolysis bullosa EB 52 vertebral subluxation 52 Mental retardation 52 chronic backache 52 suppurative 52 craniofacial abnormalities 52 Primary Sclerosing 52 Pulmonary hypertension 52 nodular melanoma 52 neurodevelopmental disability 52 Melasma 51 Arnold Chiari 51 epidermolysis bullosa 51 cleft lip cleft palate 51 SCN9A gene 51 scleroderma chronic 51 Adult Respiratory Distress 51 Transverse Myelitis 51 dermoid cyst 51 Usher syndrome 51 atrophic gastritis 51 oral thrush 51 Mitral regurgitation 51 Phenylketonuria PKU 51 primary IGFD 51 Obsessive compulsive disorder 51 corneal swelling 51 motor neuropathy 51 Ménière disease 51 reflex sympathetic dystrophy 51 hereditary predisposition 51 osteogenesis 51 bacterial prostatitis 51 neurological degeneration 51 Psoriatic arthritis 51 uveitis 51 pterygium 51 idiopathic generalized epilepsy 51 hypoplastic 51 neuritic 51 bacterial endocarditis 51 polydactyly 51 Moebius Syndrome 51 CRVO 51 bony metastases 51 Ehlers Danlos Syndrome 51 mental retardation blindness 51 fatal neuromuscular disorder 51 biliary atresia 51 strabismus crossed 51 erythema nodosum 51 angiographically 51 sporadic Creutzfeldt Jakob 51 keloid scars 51 debilitating neurological disorder 51 MPGN 51 Stargardt macular dystrophy 51 neurologic symptoms 51 dystrophic 51 Li Fraumeni syndrome 51 vitreous floaters 51 congenital abnormality 51 urethral stricture 51 interrupted aortic arch 51 Morquio Syndrome 51 chromosomal defect 51 rheumatologic 51 variable immunodeficiency 51 Aortic stenosis 51 purpura 51 ophthalmologic disorders 51 Irritable bowel syndrome IBS 51 idiopathic scoliosis 51 myocarditis inflammation 51 neurodegenerative disorder 51 motor neurone 51 familial adenomatous polyposis FAP 51 bronchoalveolar 51 vascular lesion 51 gastroesophageal reflux GERD 51 papilledema 51 malformation 51 geographic atrophy 51 Essential tremor 51 Lennox Gastaut Syndrome 51 Diamond Blackfan anemia 51 proximal femoral focal 51 degenerative 51 microscopic colitis 51 neuromotor 51 OSAHS 51 facial disfiguration 51 Hypoplastic Left Heart 51 uvea 51 endocrine gland 51 Rubinstein Taybi syndrome 51 artery stenosis 51 premorbid 51 Aplastic anemia 51 Presbyopia 51 biliary atresia rare 51 autoimmune hemolytic anemia 51 pleural effusion 51 cataracts clouding 51 inflammatory demyelinating 51 Scheuermann kyphosis 51 spastic diplegia cerebral palsy 51 polyneuropathy 51 Autistic Disorder 51 TMJ temporomandibular joint 51 cerebal palsy 51 biofeedback therapy 51 HELLP syndrome 51 PIDD 51 Idiopathic 51 intestinal microbiota 51 celiac sprue 51 Shwachman Diamond Syndrome 51 enlarged adenoids 51 neurological ailment 51 Retinal detachment 51 comorbid disorders 51 symptomology 51 venous disorders 51 spontaneous regression 51 prolapsed uterus 51 uncontrolled epilepsy 51 CMV retinitis 51 MELAS 51 mesenteric ischemia 51 Autoimmune disorders 51 hormonal disorder 51 tonsillar 51 cerebral palsy neurological disorder 51 neuro degenerative 51 Chronic constipation 51 progeria rare 51 chromosomal anomaly 51 primary biliary cirrhosis 51 degenerative muscular 51 anatomical abnormalities 51 Atresia 51 Pulmonary arterial hypertension 51 thunderclap headache 51 metachromatic leukodystrophy 51 polyomavirus nephropathy 51 autosomal recessive 51 ARVD 51 hypermobility 51 Thyroid hormone 51 hypercoagulable 51 dilated cardiomyopathy 51 swelling stiffness 51 TTTS 51 glaucomatous 51 Auditory Processing Disorder 51 Dwarfism 51 geographic atrophy GA 51 craniofacial defects 51 thrombophilia 51 monogenic 51 Chronic pelvic 51 pseudophakic 51 Maroteaux Lamy Syndrome 51 biochemical imbalance 51 retrograde amnesia 51 parathyroid 51 DiGeorge syndrome 51 myelodysplasia 51 APOE genotype 51 neuropsychological functioning 51 blocked fallopian tubes 51 acute myocarditis 51 neuropathologic 51 swallowing disorders 51 mitral valve regurgitation 51 CFS ME 51 exotropia 51 tumoral 51 skeletal deformities 51 Chronic fatigue 51 developmental abnormalities 51 psychogenic 51 cirrhotic liver 51 dementia praecox 51 reactive airway 51 biventricular failure 51 acute myocardial ischemia 51 sonographic appearance 51 Takayasu arteritis 51 cerumen impaction 51 corneal infections 51 juvenile idiopathic arthritis 51 periventricular leukomalacia 51 skeletal malformations 51 hydronephrosis 51 lung fibrosis 51 dementing 51 Iwach 51 seizure disorders 51 muscle degeneration 51 hyperplastic 51 spondylitis 51 Moyamoya disease 51 polycystic ovaries 51 hereditary blindness 51 Tychsen 51 chromosome #q#.# deletion 51 lumbosacral 51 patellar dislocation 51 bladder exstrophy 51 autosomal dominant 51 filaggrin 51 Coeliac disease 51 nonprogressive 51 degenerative nerve 51 hemorrhagic colitis 51 myalgias 51 ASPD 51 Alopecia Areata 51 degenerative neuromuscular disease 51 osteosarcoma bone 51 Friedreich 51 Cornea transplants 51 Kufs disease 51 spondyloarthritis 51 Vingan 51 tracheal stenosis 51 mastocytosis 51 neurological sequelae 51 precancerous condition 51 joint contractures 51 maculopathy 51 hypogonadotropic hypogonadism 51 ciliopathies 51 Graves ophthalmopathy 51 Otitis media 51 transfusion syndrome 51 Gender Identity Disorder 51 cauda equina syndrome 51 spondylosis 51 airway hyperresponsiveness 51 imperforate anus 51 olfactory dysfunction 51 Long QT syndrome 51 amusia 51 congenital adrenal hyperplasia CAH 51 thyroid nodule 51 leptin deficiency 51 Neurocognitive 51 visual impairment 51 blastoma 50 nuchal 50 cervical degenerative disc 50 G#S mutation 50 Takotsubo cardiomyopathy 50 progressive neurodegenerative disorder 50 papillary carcinoma 50 diplopia 50 nystagmus 50 dermatosis 50 idiopathic cardiomyopathy 50 nerve entrapment 50 brachial plexus injuries 50 #q#.# deletion syndrome 50 Celiac sprue 50 Motor neurone disease 50 Aspergers Syndrome 50 neuro musculoskeletal 50 Tourette Syndrome TS 50 mental retardation cerebral palsy 50 enzyme deficiency 50 necrotising enterocolitis 50 Gastroparesis 50 anterior uveitis 50 telogen effluvium 50 epilepsy 50 androgenetic alopecia 50 hypoplasia 50 temporal lobectomy 50 pulmonary inflammation 50 pseudogout 50 choroidal melanoma 50 Wiskott Aldrich syndrome 50 fibrotic disease 50 facial paralysis 50 inherited neurological disorder 50 Gynecomastia 50 supraventricular tachycardia 50 hemangioma 50 fibrodysplasia ossificans progressiva 50 pathophysiological mechanisms 50 Niemann Pick 50 cystic fibrosis chronic pancreatitis 50 progressive multifocal PML 50 muscular dystrophy cerebral palsy 50 cerebellar 50 cystic fibrosis hereditary 50 hyperprolactinemia 50 Attention Deficit Hyperactive Disorder 50 TMJ dysfunction 50 irritation rashes 50 Genetic mutation 50 Avascular necrosis 50 schizo affective disorder 50 femoral neck fractures 50 pyoderma 50 Klinefelter syndrome 50 Reflex sympathetic dystrophy 50 Korsakoff syndrome 50 cortical atrophy 50 dysarthria 50 diverticular 50 Acute myeloid leukemia 50 fibrocystic breast 50 impingement syndrome 50 neurological abnormalities 50 autoimmune thyroid 50 cochlear implantation 50 discogenic 50 neuronal dysfunction 50 strokelike symptoms 50 gait abnormalities 50 sinonasal 50 tau pathology 50 Lichen planus 50 generalized epilepsy 50 contractures 50 nonepileptic seizures 50 thiopurine 50 Major depressive disorder 50 hyperammonemia 50 retinal edema 50 microencephaly 50 hemispherectomy 50 osteochondritis 50 motor neuron diseases 50 clinically heterogeneous 50 esophagitis 50 SNHL 50 retinal nerve 50 Guillain Barre Syndrome GBS 50 membranous nephropathy 50 nephrosis 50 cataract extraction 50 genetic syndromes 50 polydipsia 50 postural orthostatic tachycardia 50 Hereditary angioedema 50 hypoperfusion 50 opacities 50 dermatomyositis 50 acute subdural hematoma 50 myelomeningocele