Related by context. All words. (Click for frequent words.) 73 septo optic dysplasia 72 congenital disorder 70 brain malformation 69 congenital cataracts 69 congenital glaucoma 69 arthrogryposis 68 quadriplegic cerebral palsy 68 Crouzon syndrome 67 Hirschsprung disease 67 pulmonary atresia 66 Usher Syndrome 66 diaphragmatic hernia 66 biliary atresia rare 66 retinitis pigmentosa degenerative 66 Leber congenital amaurosis 66 ocular albinism 65 static encephalopathy 65 cardio myopathy 65 skeletal dysplasia 65 Hirschsprung Disease 65 arthrogryposis multiplex congenita 65 atresia 65 optic atrophy 65 rare chromosomal disorder 65 cortical blindness 65 Hypoplastic Left Heart 65 CHARGE syndrome 65 chiari malformation 65 aniridia 65 congenital diaphragmatic hernia 65 biliary atresia 65 degenerative disorder 64 spastic quadriplegic cerebral palsy 64 esophageal atresia 64 spastic cerebral palsy 64 congenital cataract 64 Treacher Collins syndrome 64 retinal dysfunction 64 spastic diplegia 64 Treacher Collins Syndrome 64 pulmonary stenosis 64 Ehlers Danlos syndrome 64 genetic disorder 64 truncus arteriosus 64 pigmentosa 63 imperforate anus 63 tricuspid atresia 63 retinal blastoma 63 Hurler syndrome 63 Leber congenital amaurosis LCA 63 hemophagocytic lymphohistiocytosis 63 Joubert syndrome 63 congenital 62 Crouzon Syndrome 62 blastoma 62 Erb palsy 62 Aicardi syndrome 62 cerebral palsy epilepsy 62 cerebral palsy neurological disorder 62 Krabbe Leukodystrophy 62 Neurofibromatosis type 62 celebral palsy 62 osteopetrosis 62 hydrops 62 Angelman syndrome 62 Apert syndrome 62 hypoplastic 61 polycystic kidneys 61 Retinoblastoma 61 rhabdomyosarcoma rare 61 retinoblastoma rare 61 Hutchinson Gilford progeria 61 Arnold Chiari Malformation 61 holoprosencephaly 61 Goldenhar syndrome 61 retinitis 61 retinitis pigmentosa RP 61 Goldenhar Syndrome 61 epidermolysis bullosa 61 hypotonia 61 microtia 61 DiGeorge syndrome rare 61 Chiari malformation 61 sacral agenesis 61 cavernous hemangioma 61 Morquio syndrome 61 mitochondrial myopathy 61 Von Willebrand disease 61 medium chain acyl 61 cerebral palsy 61 osteosarcoma bone 60 degenerative muscular 60 Apert Syndrome 60 detached retinas 60 congential 60 Sturge Weber syndrome 60 juvenile dermatomyositis 60 spinal bifida 60 neurofibromatosis genetic disorder 60 fibrous dysplasia 60 bilateral retinoblastoma 60 cerebri 60 Leber Congenital Amaurosis LCA 60 paralysis blindness 60 optic nerves 60 bone deformities 60 apraxia 60 Wilm tumor 60 osteogenesis imperfecta 60 hereditary hemorrhagic telangiectasia 60 Ewing sarcoma bone 60 hypothalamic hamartoma 60 cerebal palsy 60 retinal dystrophy 60 pyloric stenosis 60 DiGeorge Syndrome 60 Hurler Syndrome 60 Ventricular Septal Defect 60 prematurity ROP 60 Perthes disease 60 Leber Congenital Amaurosis 60 spastic quadriplegia 60 chromosome abnormality 60 incurable neurological disorder 60 malformation 60 Crigler Najjar syndrome 60 congenital scoliosis 60 congenital muscular dystrophy 60 dysgenesis 59 juvenile myelomonocytic leukemia 59 Dysplasia 59 Moebius syndrome 59 hemangioma 59 brachial plexus palsy 59 cleft lip palate 59 Rubinstein Taybi syndrome 59 incurable genetic 59 retinitis pigmentosa hereditary 59 optic nerve atrophy 59 Beckwith Wiedemann Syndrome 59 proximal femoral focal 59 dermoid cyst 59 dilated cardiomyopathy 59 Treacher Collins 59 DiGeorge syndrome 59 cleft palette 59 degenerative neurological disorder 59 ectodermal dysplasia 59 cerebral thrombosis 59 psychosocial dwarfism 59 hydrocephaly 59 chronic granulomatous disease 59 Proteus Syndrome 59 atrial septal defect 59 mental retardation blindness 59 retinal bleeding 59 metachromatic leukodystrophy 59 Cerebral palsy 59 pseudotumor cerebri 59 chromosomal disorder 59 corneal scarring 59 autosomal recessive genetic 59 Retinopathy 59 atrioventricular septal defect 59 bladder exstrophy 59 neurofibromatosis 59 Moebius Syndrome 59 clubfeet 59 neurogenic bladder 59 cystic kidney 59 Severe Combined Immunodeficiency 59 Stargardt Macular Dystrophy 59 facial palsy 59 epidermolysis bullosa EB 59 Duchene muscular dystrophy 59 Chiari Malformation 58 leukodystrophy 58 congenital deformity 58 Retinitis pigmentosa 58 Sanfilippo Syndrome 58 Alport syndrome 58 recessive dystrophic epidermolysis bullosa 58 stem glioma 58 Arnold Chiari 58 diabetes insipidus 58 Wolf Hirschhorn 58 hemiparesis 58 primary ciliary dyskinesia 58 Biliary Atresia 58 chromosomal defect 58 retinal hemorrhage 58 dystonia neurological movement 58 dominantly inherited 58 syringomyelia 58 Sanfilippo syndrome 58 hemiplegia 58 venous malformation 58 debilitating neurological disease 58 Wilms Tumor 58 Joubert Syndrome 58 Churg Strauss syndrome 58 hereditary disorder 58 idiopathic cardiomyopathy 58 diffuse intrinsic pontine glioma 58 Beckwith Wiedemann syndrome 58 persistent pulmonary hypertension 58 cortical dysplasia 58 hereditary degenerative 58 Dravet syndrome 58 curved spine 58 blood clotting disorder 58 epilepsy neurological disorder 58 Krabbe Disease 58 Lennox Gastaut Syndrome 58 spina bifada 58 twin transfusion 58 progressive retinal degenerative 58 spastic paraplegia 58 congenital hydrocephalus 58 Henoch purpura 58 Krabbe disease 58 Arteriovenous Malformation 58 osteogenic sarcoma 58 hypoplasia 58 achromatopsia 58 cerebral edema swelling 58 enzyme deficiency 58 cerebellar ataxia 58 posterior urethral valves 58 spina bifida defect 58 vascular malformation 58 degenerative retinal disease 57 ventricular septal defect VSD 57 Stargardt macular dystrophy 57 paresis 57 hereditary spastic paraplegia 57 Neurofibromatosis Type 57 transfusion syndrome 57 limb deformities 57 DIPG 57 cystic hygroma 57 severely impairs 57 Diffuse Intrinsic Pontine Glioma 57 cerebral palsy mental retardation 57 Hypertrophic 57 neurodevelopmental disorder 57 congenital insensitivity 57 embryonal rhabdomyosarcoma 57 severe aplastic anemia 57 corneal edema 57 Pompe disease rare 57 heterotaxy 57 Benign Paroxysmal Positional Vertigo 57 degenerative nerve 57 Charcot foot 57 Wilms tumor 57 achondroplasia 57 polycystic kidney disease 57 Proteus syndrome 57 thyroiditis 57 fibromatosis 57 Down syndrome chromosomal disorder 57 dysphasia 57 neurological disorder affecting 57 verbal apraxia 57 amblyopia lazy eye 57 HELLP syndrome 57 Pelizaeus Merzbacher disease 57 hydrocephalus 57 intercranial 57 dyspraxia 57 progressive neuromuscular 57 velo cardio facial 57 Wilms Tumour 57 Maroteaux Lamy Syndrome 57 juvenile rheumatoid arthritis 57 noncancerous tumor 57 otosclerosis 57 myotonic dystrophy 57 craniofacial deformities 57 intractable epilepsy 57 neuromotor 57 Klippel Trenaunay Weber 57 neuro degenerative 57 fatal neurodegenerative disorder 57 neurodevelopment disorder 57 Cockayne syndrome 57 congenital abnormality 57 Tourette Syndrome neurological disorder 57 Holoprosencephaly 57 leukoencephalopathy 57 Sclerosing 57 nonarteritic anterior ischemic optic 57 pulmonary thromboembolism 57 Noonan Syndrome 57 degenerative neurological disease 57 aplastic anemia rare 57 underdeveloped lungs 57 Tetralogy 57 bacterial endocarditis 57 Meniere Disease 57 uterus didelphys 57 reflex sympathetic dystrophy 57 tracheal stenosis 57 Optic nerve 57 Ewings Sarcoma 57 rhabdomyosarcoma 56 ventricular septal defect 56 Ebstein anomaly 56 chromosome #q#.# deletion 56 autosomal dominant polycystic kidney 56 spinal meningitis 56 born profoundly deaf 56 idiopathic dilated cardiomyopathy 56 autistic tendencies 56 mental retardation cerebral palsy 56 retinitis pigmentosa 56 tuberous sclerosis 56 gene MECP2 56 cranio 56 surgically corrected 56 fallot 56 cerebellar hypoplasia 56 agenesis 56 Myocarditis 56 spina bifida birth 56 strabismus crossed 56 myelomeningocele 56 dyskeratosis congenita 56 spondylolysis 56 Fanconi anemia 56 Hutchinson Gilford Progeria Syndrome 56 coarctation 56 Usher syndrome 56 lissencephaly 56 progressive neurodegenerative disorder 56 Hutchinson Gilford Progeria 56 pontine glioma 56 hormonal disorder 56 Cleft palate 56 craniofacial defects 56 multiorgan 56 Macular degeneration 56 Parkinsons Disease 56 enterocolitis 56 anterior ischemic optic neuropathy 56 Langerhans cell histiocytosis 56 aplasia 56 spina bifida 56 Wilms tumors 56 neurocysticercosis 56 Parkinson disease degenerative 56 Angelman Syndrome 56 nerve palsy 56 diseases chronic granulomatous 56 metabolic disorder 56 optic neuropathy 56 anoxic brain injury 56 recessive genetic 56 myelopathy 56 Lafora disease 56 Ectopia Cordis 56 polyhydramnios 56 Budd Chiari syndrome 56 Sandhoff disease 56 cerebral palsey 56 Alagille syndrome 56 abdominal abscesses 56 profound deafness 56 Osteogenesis Imperfecta 56 spastic paralysis 56 Retinitis Pigmentosa RP 56 esotropia 56 multisystem disease 56 pulmonary hypoplasia 56 Pervasive Developmental Disorder 56 Prader Willi syndrome 56 periventricular leukomalacia 56 cataracts glaucoma 56 dehydration malnutrition 56 rare neurological disorder 56 neuroblastoma tumor 56 nonalcoholic cirrhosis 56 optic neuritis 56 cardiomyopathy weakening 55 BH4 deficiency 55 epidural abscess 55 retinal haemorrhage 55 petit mal seizures 55 Juvenile Rheumatoid Arthritis 55 inherited retinal degeneration 55 congenital blindness 55 neurofibromatosis NF 55 Wiskott Aldrich Syndrome 55 osteogenesis 55 retinoblastoma cancerous tumor 55 retinoblastoma 55 restrictive cardiomyopathy 55 congenital achromatopsia 55 dysautonomia 55 auditory neuropathy 55 Congenital 55 muscular atrophy 55 optic nerve 55 retinal degeneration 55 degenerative neuromuscular disease 55 discoid lupus 55 transverse myelitis 55 retinal pigment epithelium 55 heart syndrome HLHS 55 Becker muscular dystrophy 55 Long QT syndrome 55 acute psychosis 55 thoracic aortic aneurysm 55 congenital cardiac 55 neurological dysfunction 55 Pompe Disease 55 spinal muscular atrophy 55 cyclic vomiting syndrome 55 Sturge Weber 55 toxemia 55 alpha1 antitrypsin deficiency 55 retinal haemorrhages 55 mitral valve regurgitation 55 dissecans 55 congenital deficiency 55 Combined Immune Deficiency 55 Tourette syndrome neurological disorder 55 intestinal pseudo 55 mental retardation epilepsy 55 systemic scleroderma 55 Sturge Weber Syndrome 55 Bi Polar Disorder 55 cataracts 55 galactosemia 55 Wilm Tumor 55 neurodegenerative disorder 55 dysgraphia 55 eosinophilic esophagitis 55 Leber Hereditary Optic Neuropathy 55 autoimmune encephalitis 55 deformity 55 pulmonary valve stenosis 55 alveolar rhabdomyosarcoma 55 Klippel Trenaunay Syndrome 55 meningeal 55 nonfunctioning kidneys 55 Apraxia 55 imperfecta 55 Fanconi anemia rare 55 bronchopulmonary dysplasia 55 airway blockage 55 neurological 55 fibroma 55 myelodysplasia 55 blindness paralysis 55 subdural hemorrhaging 55 motor neuropathy 55 placental abruption 55 osteogenesis imperfecta OI 55 joint contractures 55 chronic venous insufficiency 55 omphalocele 55 thyroid hormone deficiency 55 neuro degenerative disorder 55 incurable degenerative 55 hypoxic ischemic encephalopathy 55 intracerebral bleed caused 55 Otitis 55 Lesch Nyhan syndrome 55 Moyamoya 55 hypoplastic left 55 craniopagus parasiticus 55 Arthrogryposis 55 inherited neurodegenerative 55 Raynaud disease 55 choriocarcinoma 54 progressive neurologic 54 Brugada Syndrome 54 Rathke cleft cyst 54 arteriovenous malformations 54 spasmodic dysphonia 54 spina bifida cerebral palsy 54 neonatal respiratory distress 54 fetal echocardiogram 54 polycystic 54 fibrodysplasia ossificans progressiva FOP 54 enlarged spleen 54 lymphoblastic lymphoma 54 pulmonary haemorrhage 54 lymphatic malformation 54 infantile spasms 54 RPE# 54 congenital heart 54 Alport Syndrome 54 congenital kidney 54 neuromuscular disorder 54 developmental delays 54 leukoencephalopathy PML 54 Perthes Disease 54 degenerative spinal 54 sudden sensorineural hearing 54 Epidermolysis bullosa 54 subdural bleeding 54 retinal detachment 54 MCAD deficiency 54 neuritis 54 Marfan Syndrome 54 myopia nearsightedness 54 congenital amputation 54 lymphangioleiomyomatosis LAM 54 myoclonic epilepsy 54 Niemann Pick disease 54 moyamoya 54 herpes encephalitis 54 Avascular necrosis 54 teratoma 54 nephritis 54 birth defect 54 neuro developmental 54 infantile hemangiomas 54 Spina bifida 54 Myasthenia gravis 54 Motor neurone disease 54 hypophosphatasia 54 lactase deficiency 54 Rett syndrome neurological disorder 54 hypoxic encephalopathy 54 Fibrous Dysplasia 54 Hip dysplasia 54 histiocytosis 54 skeletal malformations 54 paraneoplastic 54 muscle degeneration 54 Diabetic neuropathy 54 adenoid 54 hyperemesis 54 Atresia 54 Frontal lobe 54 bicuspid valve 54 Spinal muscular atrophy 54 Prematurity ROP 54 inherited retinal 54 fatal myelination disorder 54 cystic fibrosis chronic pancreatitis 54 dyskinetic 54 inoperable tumor 54 Parkinson degenerative 54 cleft lip cleft palate 54 exotropia 54 angiosarcoma 54 aplastic anemia 54 Histiocytosis 54 glomerulonephritis 54 spinocerebellar ataxia 54 Eisenmenger syndrome 54 Battens Disease 54 Mitochondrial disease 54 mitochondrial disease 54 Stargardt disease 54 NF2 54 cystic fibrosis Duchenne muscular 54 profoundly deaf 54 dystrophy 54 variable immunodeficiency 54 Izabelle 54 spastic diplegia cerebral palsy 54 cholestasis 54 subarachnoid haemorrhage 54 entropion 54 Acute Myelogenous Leukemia 54 neurofibroma 54 dysarthria 54 cardiovascular restenosis cancer 54 neurological disorder 54 polycystic ovarian disease 54 interstitial nephritis 54 skeletal deformities 54 borderline mental retardation 54 hypokalemia hypomagnesemia 54 ruptured brain aneurysm 54 polymyalgia 54 Langerhans Cell Histiocytosis 54 severe malignant osteopetrosis 54 glycogen storage 54 glaucoma cataract 54 neuropsychiatric disorder 54 multisystem disorder 54 muscle hypertrophy 54 temporal lobectomy 53 Osgood Schlatter disease 53 Iron deficiency anemia 53 hemorrhagic pancreatitis 53 Medulloblastoma 53 neurogenetic 53 amblyopia 53 idiopathic thrombocytopenic purpura 53 excruciating headaches 53 colic diarrhea 53 metabolic abnormality 53 Osteogenesis imperfecta 53 hereditary deafness 53 Transverse Myelitis 53 clotting disorder 53 genetically inherited 53 defects mental retardation 53 corneal epithelial 53 pituitary adenoma 53 undiagnosed celiac disease 53 Angelman 53 venous thoracic outlet 53 syndrome FAS 53 Sudden Arrhythmic Death 53 congenital adrenal hyperplasia CAH 53 renal kidney 53 bronchopneumonia 53 Fragile X Syndrome 53 thyroid deficiency 53 Canavan Disease 53 myotonic muscular dystrophy 53 desmoid tumor 53 asperger syndrome 53 McCune Albright 53 Schwannoma tumor 53 epilepsy 53 fractured ribs lacerated liver 53 acute subdural hematoma 53 ANCA associated 53 vascular abnormality 53 autosomal dominant disorder 53 immuno deficiency 53 congenital defects 53 multi infarct dementia 53 primary pulmonary hypertension 53 vertebral artery dissection 53 microcephaly 53 debilitating neurological disorder 53 Rhabdomyosarcoma 53 Diamond Blackfan Anemia 53 dysphonia 53 lysosomal storage disease 53 chronic idiopathic 53 ataxia telangiectasia 53 orthostatic intolerance 53 blindness deafness 53 RDEB 53 abnormal genital 53 rare autosomal recessive 53 progressive neurological disorder 53 interrupted aortic arch 53 multiforme 53 brain hemorrhages 53 myasthenia gravis 53 Stenosis 53 neurodegenerative disorder characterized 53 nephropathy kidney 53 lymphoblastic leukemia 53 acute myocarditis 53 hemispherectomy 53 wet macular degeneration 53 arteriovenous malformation 53 neuro muscular disorder 53 immunodeficiency disorder 53 pancreatitis inflammation 53 genetic defect 53 Essential tremor 53 paraganglioma 53 hyperinsulinism 53 autoimmune intestinal 53 neuro developmental disorder 53 Fanconi Anemia 53 anencephaly fatal 53 congenital hypothyroidism 53 hyperreflexia 53 phenylketonuria 53 WAGR syndrome 53 neurobiological disorder 53 cardiac insufficiency 53 idiopathic pulmonary 53 degenerative neurological 53 sensorineural hearing loss 53 ischemic bowel 53 Arrhythmogenic Right Ventricular Cardiomyopathy 53 Rhabdomyosarcoma rare 53 Myotonic dystrophy 53 Irlen Syndrome 53 Morquio Syndrome 53 facial deformity 53 uremia 53 epilepsy neuro oncology 53 retinal hemorrhaging 53 HELLP 53 choroidal melanoma 53 pulmonary alveolar 53 Severe Primary IGFD 53 supraventricular tachycardia 53 fat malabsorption 53 spontaneous pneumothorax 53 renal failure interstitial lung 53 congenital anomaly 53 celiac sprue disease 53 Fuchs dystrophy 53 Asberger syndrome 53 Duchene Muscular Dystrophy 53 neurocardiogenic syncope 53 Parkinsons disease 53 intracranial haemorrhage 53 progressive neurodegenerative 53 meningitis encephalitis pulmonary edema 53 Benign prostatic hyperplasia 53 craniofacial abnormalities 53 interstitial fibrosis 53 Acute Leukemia 53 shunt implanted 53 congenital disorders 53 neurofibromatosis type 53 cleft pallet 53 Niemann Pick 53 nephrotic syndrome 53 corneal ulcer 53 vascular malformations 53 Friedrich Ataxia 53 cystic fibrosis hereditary 53 Trigeminal neuralgia 53 Dwarfism 53 patent ductus arteriosus 53 incompetent cervix 53 anencephaly 53 autism neurological disorder 53 ruptured ectopic pregnancy 53 intracranial hemorrhage bleeding 53 vascular birthmarks 52 Krabbe leukodystrophy 52 immunodeficiencies 52 valvular heart disease 52 Nephrotic Syndrome 52 disorder characterized 52 rhabdomyosarcoma rare cancer 52 contractures 52 inappropriate antidiuretic hormone SIADH 52 fatal neurodegenerative 52 Smith Lemli Opitz 52 abnormal curvature 52 craniosynostosis 52 adenomyosis 52 bicuspid aortic valve 52 lichen planus 52 Pulmonary hypertension 52 expressive aphasia 52 cerebellar 52 post transplant lymphoproliferative 52 molar pregnancy 52 perinatal asphyxia 52 hypertrichosis 52 limbal stem cell 52 microencephaly 52 Factor XIII 52 ruptured uterus 52 ventricular dilation 52 muscular spasticity 52 Acute Myeloid Leukaemia 52 Meckel Gruber 52 congenital malformation 52 dystonia neurological disorder 52 chromosomal abnormality 52 muscle spasticity 52 chromosomal anomaly 52 acute colitis 52 Beta thalassemia 52 Childhood Disorder 52 Anencephaly 52 hypertrophic obstructive cardiomyopathy 52 aplastic 52 surgeons implanted 52 ataxia 52 Atrial Septal Defect 52 cerebral palsy autism 52 Nonspecific 52 Asperger Disorder 52 disorder thalassemia 52 neonatal encephalopathy 52 dizziness numbness 52 prosopagnosia 52 levodopa induced 52 Acute Lymphocytic Leukemia 52 Fatty liver 52 chronic autoimmune disorder 52 Aspergers Syndrome 52 muscular dystrophy cerebral palsy 52 serotonin imbalance 52 mesenteric ischemia 52 fibrodysplasia ossificans progressiva 52 manic depressive disorder 52 6 phosphate dehydrogenase 52 arthropathy 52 ruptured bowel 52 rediagnosed 52 Burkitt Lymphoma 52 lobar pneumonia 52 neurologic deficits 52 leptin deficiency 52 pilocytic astrocytoma 52 hereditary blindness 52 torticollis 52 dwarfism 52 coagulopathy 52 Pancreatic insufficiency 52 Korsakoff syndrome 52 umbilical hernia 52 malformations 52 supranuclear palsy 52 artery stenosis 52 sympathetic ophthalmia 52 intraventricular hemorrhage 52 hemolytic disease 52 Gastroparesis 52 neurofibromas 52 myotonia 52 AML Leukemia 52 Retinitis Pigmentosa 52 respiratory insufficiency 52 ischemic colitis 52 Bacterial vaginosis 52 deformed limbs 52 postural orthostatic tachycardia 52 plexiform 52 Obstetric fistula 52 Reflex sympathetic dystrophy 52 bowel bladder 52 spinal deformities 52 spinal deformity 52 infantile hemangioma 52 underactive thyroid gland 52 Lennox Gastaut syndrome 52 primordial dwarfism 52 aortic valve stenosis 52 wears prosthetic 52 systemic amyloidosis 52 myelitis 52 haemolytic uraemic syndrome 52 Astrocytoma 52 myocarditis inflammation 52 deafness neurological 52 Fanconi Anaemia 52 osteochondritis dissecans 52 interstitial pneumonitis 52 edema swelling 52 progressive multifocal PML 52 macular degeneration glaucoma 52 Osgood Schlatter 52 progeria rare 52 cerebral aneurysm 52 Intussusception 52 Prenatal diagnosis 52 stimulator implanted 52 Stargardt Disease 52 severe scoliosis curvature 52 diffuse pontine glioma 52 mastocytosis 52 scoliosis 52 Fanconi anemia FA 52 Graves ophthalmopathy 52 Aortic stenosis 52 Down syndrome cerebral palsy 52 muscular degeneration 52 roseola 52 Wegener Granulomatosis 52 primitive neuroectodermal tumors 52 dystonia 52 urethral stricture 52 neurotology neuropsychology headaches 52 MELAS 52 brain aneurism 52 acute lymphatic leukemia 52 cochlear implantation 52 adrenoleukodystrophy ALD 52 disfigurations birthmarks 52 polycystic kidney 52 headaches nausea vomiting 52 enlarged thyroid gland 52 renovascular hypertension 52 Von Willebrand 52 ischemic optic neuropathy 52 myasthenia gravis neuromuscular 52 hip dysplasia 52 SNHL 52 situs inversus 52 superior mesenteric artery 52 hypertrophic cardiomyopathy HCM 52 streptococcus infection 52 Congenital Muscular Dystrophy 52 neuritic 52 deafness blindness 52 chronic renal insufficiency 52 shunt inserted 52 Dravet Syndrome 52 autoimmune thyroiditis 52 dermoid 52 chronic obstructive airway 52 Dravet 52 purpura 52 Huntington Chorea 52 lymphocytic leukemia 52 Leber hereditary optic neuropathy 52 MPGN 52 transient quadriplegia temporary 52 induced cardiomyopathy 52 Diamond Blackfan anemia 52 venous drainage 51 benign positional vertigo 51 maple syrup urine 51 myxedema 51 skull fractures bleeding 51 neonatal jaundice 51 thymus gland 51 congenital birth defects 51 bullous 51 drooping eyelid 51 neuro muscular 51 Patau syndrome 51 chronic rheumatic 51 Amblyopia 51 nystagmus 51 dilated cardiomyopathy DCM 51 atypical rhabdoid tumor 51 Spinal cord 51 arteriovenous malformation AVM 51 lipoma 51 Morton Neuroma 51 malnutrition dehydration 51 hyphema 51 complement inhibitor eculizumab 51 ceroid lipofuscinosis NCL 51 degenerative 51 genetic neuromuscular disorder 51 hypertensive retinopathy 51 idiopathic epilepsy 51 impaired cognition 51 developmental disorder 51 β thalassemia 51 von Willebrand disease 51 macular dystrophy 51 dermopathy 51 nerve degeneration 51 neovascularisation 51 subependymal giant cell 51 Hemochromatosis 51 hepatoblastoma 51 viral myocarditis 51 ependymoma 51 Hashimoto thyroiditis 51 degenerative disorders 51 degenerative neurological condition 51 nephrosis 51 retinal 51 recurrent laryngeal nerve 51 angioma 51 brittle bone 51 polyneuropathy 51 opsoclonus myoclonus syndrome 51 peripheral neuropathy nerve 51 Coeliac disease 51 Hodgkins Lymphoma 51 congenital deafness 51 hippocampal function 51 juvenile myoclonic epilepsy 51 abdominal hernia 51 amniotic fluid embolism 51 Cleft lip 51 Ewings sarcoma 51 precocious puberty 51 beta thalassemia 51 peripartum cardiomyopathy 51 Myasthenia 51 Muscular dystrophy 51 urinary blockage 51 Polycystic Ovary Syndrome 51 spinal muscular atrophy SMA 51 eosinophilic 51 autosomal recessive 51 bone deformity 51 TMJ temporomandibular joint 51 strabismus 51 congenital brain tumor 51 Mermaid Syndrome 51 maculopathy 51 SIADH 51 Phenylketonuria PKU 51 crohn disease 51 Shwachman Diamond Syndrome 51 Congenital Adrenal Hyperplasia 51 cochlear nerve 51 adrenal function 51 Foetal alcohol 51 Asberger Syndrome 51 enlarged adenoids 51 inherited neurological disorder 51 akinesia 51 bowel perforation