Related by context. All words. (Click for frequent words.) 73 arthrogryposis 72 optic nerve hypoplasia 71 septo optic dysplasia 70 atresia 69 genetic disorder 69 brain malformation 68 Joubert syndrome 68 diaphragmatic hernia 67 malformation 67 sacral agenesis 67 Crouzon syndrome 67 congenital deformity 67 Hirschsprung Disease 67 pulmonary atresia 67 chromosomal disorder 66 chromosomal defect 66 birth defect 66 limb deformities 66 congenital glaucoma 66 spastic diplegia 66 biliary atresia 65 truncus arteriosus 65 chromosome abnormality 65 degenerative disorder 65 hormonal disorder 65 Goldenhar syndrome 65 Apert syndrome 65 pulmonary stenosis 65 holoprosencephaly 65 rare chromosomal disorder 65 genetic defect 65 deformity 65 hypoplasia 65 congenital diaphragmatic hernia 65 congenital abnormality 65 congenital anomaly 64 spastic cerebral palsy 64 congenital 64 bone deformities 64 epidermolysis bullosa 64 Goldenhar Syndrome 64 skeletal dysplasia 64 DiGeorge syndrome rare 64 Hirschsprung disease 64 Ventricular Septal Defect 64 Treacher Collins syndrome 64 cardio myopathy 64 Perthes disease 64 vascular malformation 63 Ehlers Danlos syndrome 63 osteopetrosis 63 esophageal atresia 63 quadriplegic cerebral palsy 63 arthrogryposis multiplex congenita 63 pyloric stenosis 63 Hypoplastic Left Heart 63 Arthrogryposis 63 hereditary disorder 63 Crouzon Syndrome 63 DiGeorge Syndrome 63 Krabbe Leukodystrophy 63 congenital cataracts 63 congenital disorders 63 imperforate anus 63 congenital malformation 63 Beckwith Wiedemann Syndrome 63 epidermolysis bullosa EB 62 ventricular septal defect 62 Spina bifida 62 osteogenesis imperfecta 62 microtia 62 congenital defect 62 DiGeorge syndrome 62 tricuspid atresia 62 degenerative neurological disorder 62 achondroplasia 62 Retinoblastoma 62 atrial septal defect 62 enzyme deficiency 62 lymphatic malformation 62 Hurler syndrome 62 hydrops 62 spina bifida 62 myelomeningocele 61 Moebius Syndrome 61 Aicardi syndrome 61 polycystic kidneys 61 fibromatosis 61 Fanconi anemia 61 hip dysplasia 61 neural tube defect 61 brachial plexus palsy 61 static encephalopathy 61 craniopagus parasiticus 61 blood clotting disorder 61 Proteus syndrome 61 retinal dysfunction 61 fibrous dysplasia 61 bladder exstrophy 61 Beckwith Wiedemann syndrome 61 cleft palette 61 cerebral palsy 60 syringomyelia 60 Angelman syndrome 60 anencephaly 60 hydrocephaly 60 Congenital 60 Klippel Trenaunay Syndrome 60 genetic abnormality 60 Leber congenital amaurosis 60 deformed limbs 60 amniotic fluid embolism 60 dilated cardiomyopathy 60 Erb palsy 60 Tetralogy 60 metabolic disorder 60 hemangioma 60 lissencephaly 60 Diamond Blackfan anemia 60 sirenomelia 60 congenital hypothyroidism 60 NF2 60 tuberous sclerosis 60 Dravet syndrome 60 mitochondrial disease 60 medium chain acyl 59 Dysplasia 59 malformations 59 agenesis 59 incompetent cervix 59 chromosomal abnormality 59 curved spine 59 Apert Syndrome 59 Chiari malformation 59 retinal blastoma 59 Biliary Atresia 59 osteogenesis imperfecta OI 59 severe aplastic anemia 59 CHARGE syndrome 59 ventricular septal defect VSD 59 Pompe disease rare 59 situs inversus 59 Wilms Tumor 59 Leber Congenital Amaurosis LCA 59 spinocerebellar ataxia 59 cerebal palsy 59 Morquio syndrome 59 chiari malformation 59 Alagille syndrome 59 Sanfilippo syndrome 59 spastic quadriplegia 59 Treacher Collins Syndrome 59 blastoma 59 Hip dysplasia 59 ectodermal dysplasia 59 optic atrophy 59 congenital defects 59 choriocarcinoma 59 spinal bifida 59 Anencephaly 59 Usher Syndrome 59 beta thalassemia 59 myelopathy 59 Proteus Syndrome 59 cerebral palsy neurological disorder 58 Holoprosencephaly 58 cerebellar ataxia 58 muscle degeneration 58 umbilical hernia 58 dermoid cyst 58 degenerative neuromuscular disease 58 ectopia cordis 58 chronic granulomatous disease 58 congenital abnormalities 58 cortical dysplasia 58 Wilm tumor 58 neurodevelopmental disorder 58 Wilms tumor 58 neurofibromatosis 58 congenital cataract 58 Sturge Weber syndrome 58 Cerebral palsy 58 dysgenesis 58 Osteogenesis Imperfecta 58 coarctation 58 osteosarcoma bone 58 dominantly inherited 58 clotting disorder 58 Noonan Syndrome 58 cystic hygroma 58 fatal neurodegenerative 58 toxemia 58 hypoplastic 58 hypothalamic hamartoma 58 craniosynostosis 58 Hurler Syndrome 58 neuritis 58 atrioventricular septal defect 58 heart syndrome HLHS 58 spastic paraplegia 58 Obstetric fistula 58 primary ciliary dyskinesia 58 hypotonia 58 Ewing sarcoma bone 58 polydactyly 58 congenital kidney 58 neuroblastoma tumor 58 Cleft palate 58 neuro muscular disorder 58 Cockayne syndrome 57 congenital scoliosis 57 pigmentosa 57 fibroma 57 clubfeet 57 Krabbe Disease 57 severely deformed 57 torticollis 57 Pulmonary hypertension 57 leukoencephalopathy 57 hemophagocytic lymphohistiocytosis 57 neurodevelopment disorder 57 deformities 57 polyhydramnios 57 dystrophy 57 Ectopia Cordis 57 acute colitis 57 entropion 57 biliary atresia rare 57 hydrocephalus 57 MCAD deficiency 57 degenerative neurological disease 57 bronchopneumonia 57 developmental abnormalities 57 autosomal recessive disorder 57 bilateral retinoblastoma 57 genetic neuromuscular disorder 57 cerebellar hypoplasia 57 Klippel Trenaunay Weber 57 molar pregnancy 57 congenital adrenal hyperplasia CAH 57 rhabdomyosarcoma 57 Rhabdomyosarcoma 57 skeletal malformations 57 microcephaly 57 patent ductus arteriosus 57 venous malformation 57 hemolytic disease 57 Leber congenital amaurosis LCA 57 Compartment syndrome 57 Arnold Chiari Malformation 57 Brugada Syndrome 57 Avascular necrosis 57 paresis 57 craniofacial abnormalities 57 autosomal dominant disorder 57 juvenile rheumatoid arthritis 57 diseases chronic granulomatous 57 neurocysticercosis 57 recessive dystrophic epidermolysis bullosa 57 spina bifida defect 57 idiopathic 57 posterior urethral valves 57 nonalcoholic cirrhosis 57 fatal neurodegenerative disorder 57 congenital birth defects 57 Hutchinson Gilford Progeria Syndrome 57 joint contractures 57 transfusion syndrome 56 discoid lupus 56 retinal hemorrhage 56 primary pulmonary hypertension 56 necrotising 56 craniofacial deformities 56 congenital hydrocephalus 56 cortical blindness 56 spastic quadriplegic cerebral palsy 56 RDEB 56 polycystic kidney disease 56 hypertrichosis 56 fallot 56 volvulus 56 persistent pulmonary hypertension 56 neuromuscular disorder 56 Krabbe leukodystrophy 56 placenta praevia 56 Intussusception 56 uterus didelphys 56 ichthyosis 56 Fibrous Dysplasia 56 hereditary hemorrhagic telangiectasia 56 immunodeficiency disorder 56 ambiguous genitalia 56 dyskeratosis congenita 56 congenital anomalies 56 scoliosis curvature 56 ocular albinism 56 autosomal recessive genetic 56 Osteosarcoma 56 primordial dwarfism 56 disease epidermolysis bullosa 56 recessive genetic 56 subdural bleeding 56 Tay Sachs disease 56 ruptured uterus 56 cavernous hemangioma 56 corneal ulcer 56 pseudotumor cerebri 56 Degenerative disc disease 56 periventricular leukomalacia 56 infantile hemangiomas 56 Fragile X Syndrome 56 neonatal respiratory distress 56 Pre eclampsia 56 spina bifida birth 56 Retinopathy 56 polydactylism 56 profound deafness 56 contractures 56 detached retinas 56 precocious puberty 56 embryonal rhabdomyosarcoma 56 cerebral thrombosis 56 congenital muscular dystrophy 56 spondylolysis 56 polycystic ovaries 56 osteochondromas 56 tracheal stenosis 56 trisomy 56 noncancerous tumor 56 cleft lip palate 56 osteogenic sarcoma 56 Iron deficiency anemia 56 galactosemia 56 Hutchinson Gilford Progeria 56 Langerhans Cell Histiocytosis 56 dysplasia 56 Rubinstein Taybi syndrome 56 leukodystrophy 56 variable immunodeficiency 56 bowel perforation 55 Combined Immune Deficiency 55 disorder thalassemia 55 twin transfusion 55 neurofibroma 55 arthropathy 55 incurable genetic 55 cranio 55 BH4 deficiency 55 trachea windpipe 55 imperfecta 55 progeria rare 55 uterine prolapse 55 Sanfilippo Syndrome 55 Down syndrome chromosomal disorder 55 dermopathy 55 bacterial endocarditis 55 Osteogenesis imperfecta 55 nerve palsy 55 defects CHDs 55 congenital heart 55 neurologic deficits 55 progressive degeneration 55 Morquio Syndrome 55 limb deformity 55 cerebri 55 uremia 55 corneal opacity 55 Hypertrophic 55 juvenile dermatomyositis 55 hemiparesis 55 neurological disorder 55 Langerhans cell histiocytosis 55 Medulloblastoma 55 congenital blindness 55 Mermaid Syndrome 55 Henoch purpura 55 debilitating neurological disorder 55 neurofibromas 55 thyroiditis 55 immunodeficiency 55 rhabdomyosarcoma rare 55 placental abruption 55 underdeveloped lungs 55 juvenile myelomonocytic leukemia 55 Coeliac disease 55 Retinitis Pigmentosa RP 55 brain hemorrhages 55 tuberous sclerosis complex 55 respiratory insufficiency 55 Aortic dissection 55 facial deformity 55 Wilm Tumor 55 Hemochromatosis 55 Congenital Adrenal Hyperplasia 55 spinal muscular atrophy 55 Myocarditis 55 spastic paralysis 55 urinary blockage 55 chromosomal anomaly 55 myotonic dystrophy 55 Arnold Chiari 55 dwarfism 55 Cystic fibrosis CF 55 neuro degenerative disorder 55 Prader Willi syndrome 55 TTTS 55 ovarian hyperstimulation syndrome 55 Hydrocephalus 55 Angelman Syndrome 55 Severe Combined Immunodeficiency 55 Rett syndrome neurological disorder 55 systemic scleroderma 55 HELLP syndrome 55 psychosocial dwarfism 55 hamartoma 55 RPE# 55 Leber hereditary optic neuropathy 55 Ebstein anomaly 55 Aplastic anemia 55 Tourette syndrome neurological disorder 55 Muscular dystrophy 55 paralytic illness 55 undescended testicle 55 subarachnoid haemorrhage 55 Chiari Malformation 55 enlarged spleen 55 Rhabdomyosarcoma rare 55 osteochondritis dissecans 55 hemiplegia 55 Klinefelter syndrome 55 necrotizing enterocolitis NEC 55 Treacher Collins 55 Hypospadias 55 hypopituitarism 55 edema swelling 55 skeletal deformities 55 intractable epilepsy 55 craniopagus 55 Cleft lip 54 Dravet Syndrome 54 diabetes insipidus 54 epididymitis 54 hypertrophic cardiomyopathy HCM 54 ADPKD 54 neurodegenerative disorder 54 primary hyperoxaluria 54 scoliosis 54 Cushing syndrome 54 teratoma 54 enlarged tonsils 54 congenital deafness 54 congential 54 Polycystic ovary syndrome 54 bone deformity 54 acute myocarditis 54 combined immunodeficiency SCID 54 retinitis 54 Battens Disease 54 motor neuropathy 54 abdominal hernia 54 heterotaxy 54 otosclerosis 54 pontine glioma 54 idiopathic cardiomyopathy 54 histiocytosis 54 Maroteaux Lamy Syndrome 54 rare neurological disorder 54 autosomal recessive 54 Hutchinson Gilford progeria 54 Transverse Myelitis 54 Wilms tumors 54 hyperemesis 54 deafness neurological 54 autosomal dominant 54 Perthes Disease 54 Lupus nephritis 54 retinoblastoma 54 inherited neurological disorder 54 diffuse intrinsic pontine glioma 54 cholestasis 54 intracranial haemorrhage 54 mitochondrial disorder 54 folic acid deficiency 54 arteriovenous malformation AVM 54 hydatid disease 54 aniridia 54 Atrial Septal Defect 54 abnormal curvature 54 fibrodysplasia ossificans progressiva FOP 54 rare congenital defect 54 cryptorchidism 54 inherited retinal degeneration 54 neonate 54 AAT deficiency 54 aneuploidies 54 Epidermolysis bullosa 54 degenerative nerve disorder 54 moyamoya 54 aortic valve stenosis 54 mitochondrial myopathy 54 enterocolitis 54 Duchene muscular dystrophy 54 AAT Deficiency 54 nonsense mutation 54 Stenosis 54 Stargardt disease 54 mucus glands 54 vertebral artery dissection 54 Neurofibromatosis type 54 Pompe Disease 54 aplasia 54 polycystic ovary syndrome 54 proximal femoral focal 54 Ewings Sarcoma 54 brachial plexus 54 desmoid tumor 54 achromatopsia 54 sensorineural hearing loss 54 spinal muscular atrophy SMA 54 bronchial pneumonia 54 Leber Congenital Amaurosis 54 Erb Palsy 54 muscular atrophy 54 polycystic 54 hereditary deafness 54 muscular degeneration 54 perinatal asphyxia 54 Marfan Syndrome 54 pulmonary hypoplasia 54 Churg Strauss syndrome 54 Hashimoto thyroiditis 54 Raynaud disease 54 Hypophosphatasia 54 Brugada syndrome 54 mental retardation blindness 54 bicuspid valve 54 Malformation 54 incurable neurological disorder 54 blindness deafness 54 chronic renal failure 54 prematurity ROP 54 lymphangioleiomyomatosis LAM 54 paraganglioma 54 leiomyosarcoma 54 Hemangiomas 54 Pelizaeus Merzbacher disease 53 long QT syndrome 53 meningoencephalitis 53 Myopathy 53 hereditary spastic paraplegia 53 metachromatic leukodystrophy 53 Sclerosing 53 Eclampsia 53 cardiomyopathy 53 Persistent Pulmonary Hypertension 53 stem glioma 53 velo cardio facial 53 juvenile myoclonic epilepsy 53 Beta thalassemia 53 endocrine disorder 53 Varicose veins 53 restrictive cardiomyopathy 53 pancytopenia 53 polymyalgia 53 ovarian cysts 53 multisystem disorder 53 ptosis 53 lactase deficiency 53 hereditary disorders 53 Joubert Syndrome 53 purpura 53 Dwarfism 53 Becker muscular dystrophy 53 clubfoot 53 spinal deformity 53 peripartum cardiomyopathy 53 systemic amyloidosis 53 coagulopathy 53 congenital deformities 53 thyroid hormone deficiency 53 cerebral palsy epilepsy 53 gangrene infection 53 arachnoiditis 53 angiosarcoma 53 streptococcus infection 53 Diamond Blackfan Anemia 53 extensor tendons 53 McCune Albright 53 achalasia 53 Necrotizing enterocolitis 53 gastroschisis 53 neonatal encephalopathy 53 carcinoid tumor 53 progressive neurodegenerative disorder 53 Moyamoya disease 53 recessive gene 53 leukoencephalopathy PML 53 paraplegia 53 retinoblastoma rare 53 cystic lesions 53 optic neuropathy 53 Bardet Biedl syndrome 53 erythema nodosum 53 benign positional vertigo 53 vasa previa 53 radiculopathy 53 dermoid 53 facial deformities 53 idiopathic generalized epilepsy 53 spontaneous pneumothorax 53 aortic rupture 53 cleft palate 53 Wiskott Aldrich Syndrome 53 anoxic brain injury 53 autism neurological disorder 53 incurable neurodegenerative disease 53 autoimmune encephalitis 53 craniofacial defects 53 hypoxic ischemic encephalopathy 53 twisted bowel 53 Osr2 53 placenta previa 53 recessive trait 53 congenital deficiency 53 ataxia telangiectasia 53 hydronephrosis 53 ruptured brain aneurysm 53 interrupted aortic arch 53 hypoplastic left 53 progressive retinal degenerative 53 Hammertoe 53 pulmonary haemorrhage 53 osteochondrosis 53 intercranial 53 Guillain Barré Syndrome 53 Essential tremor 53 Alport syndrome 53 mitral valve regurgitation 53 neurological complications 53 Aortic stenosis 53 Von Willebrand disease 53 aplastic anemia 53 thymus gland 53 Seborrheic dermatitis 53 diagnosed prenatally 53 chiari 53 cleft lip cleft palate 53 gene MECP2 53 enlarged adenoids 53 Arteriovenous Malformation 53 Retinitis pigmentosa 53 osteochondritis 53 idiopathic dilated cardiomyopathy 53 Clubfoot 53 Wolf Hirschhorn 53 genetic mutation 53 neurological disorder affecting 53 renal agenesis 53 hyperprolactinemia 53 neurogenic bladder 53 orthostatic intolerance 53 Spinal muscular atrophy 53 retinal degeneration 53 alveolar rhabdomyosarcoma 53 MCADD 53 retinitis pigmentosa hereditary 53 Myasthenia gravis 53 retinal dystrophy 53 Eisenmenger syndrome 53 retinal haemorrhage 53 Vitamin B# deficiency 53 neural tube defects NTDs 53 alopecia universalis 53 cardiomegaly 53 dysmorphic features 53 Kabuki syndrome 53 Neurofibromatosis Type 53 retinitis pigmentosa degenerative 53 digestive disorder 53 interstitial pneumonitis 53 severe malignant osteopetrosis 53 mental retardation epilepsy 53 spina bifada 53 rheumatic heart 53 developmental disorder 53 polymyalgia rheumatica 53 gene mutation 53 neurofibromatosis NF 53 polymorphic ventricular tachycardia 52 hypoxic encephalopathy 52 congenital achromatopsia 52 multisystem disease 52 congenital amputation 52 Shwachman Diamond Syndrome 52 cystic fibrosis chronic pancreatitis 52 epiglottitis 52 hyperkeratosis 52 xeroderma pigmentosum 52 pulmonary thromboembolism 52 Diffuse Intrinsic Pontine Glioma 52 cardiac tamponade 52 prolapsed 52 goitre 52 degenerative retinal disease 52 corneal edema 52 palsy 52 Acute Myeloid Leukaemia 52 facial cleft 52 glomerulonephritis 52 Fanconi Anemia 52 brachial plexus injuries 52 placenta accreta 52 Polycystic ovary syndrome PCOS 52 Ichthyosis 52 inherited mutations 52 Budd Chiari syndrome 52 Trisomy 52 irreversible blindness 52 recurrent laryngeal nerve 52 neurologic disorder 52 Dilated cardiomyopathy 52 encephalocele 52 neuro developmental disorder 52 Sandhoff disease 52 facial palsy 52 petit mal seizures 52 Usher syndrome 52 debilitating arthritis 52 vein thrombosis 52 limb malformations 52 celebral palsy 52 alpha thalassemia 52 Cystic fibrosis 52 degenerative 52 adrenoleukodystrophy ALD 52 Biliary atresia 52 Histiocytosis 52 Parkinson degenerative 52 Maroteaux Lamy syndrome 52 Fallopian tube 52 synovial sarcoma 52 haemolytic anemia 52 ischemic colitis 52 bowel obstruction 52 cardiomyopathy weakening 52 atrial septal 52 atypical rhabdoid tumor 52 intracranial hemorrhage bleeding 52 prolapsed uterus 52 progressive neuromuscular 52 pituitary adenoma 52 dystonia 52 wears prosthesis 52 intraventricular hemorrhage 52 upper airway obstruction 52 developmental dysplasia 52 ruptured bowel 52 calcium deficiency 52 Long QT syndrome 52 pyelonephritis 52 Bacterial vaginosis 52 Syndrome SADS 52 abnormalities 52 neonatal jaundice 52 cataracts 52 Polycystic kidney disease 52 hydrocele 52 Li Fraumeni syndrome 52 iritis 52 neurofibromatosis genetic disorder 52 necrotizing enterocolitis 52 Tuberous sclerosis 52 retinitis pigmentosa RP 52 inoperable tumor 52 subdural haemorrhage 52 Diabetic neuropathy 52 thyroid deficiency 52 parasitic twin 52 Von Willebrand 52 vascular abnormality 52 genetic syndromes 52 postpartum haemorrhage 52 Aicardi Syndrome 52 Pervasive Developmental Disorder 52 rheumatic disease 52 subdural hemorrhages 52 valvular heart disease 52 neuropsychiatric disorder 52 Wegener granulomatosis 52 neurological manifestations 52 PNET 52 progressive neurological disorder 52 WAGR syndrome 52 hemochromatosis 52 fibroid tumor 52 Synovial Sarcoma 52 neurological sequelae 52 HLHS 52 ventricular dysplasia 52 hemolytic anemia 52 spine curvature 52 otitis 52 idiopathic scoliosis 52 spinal muscle atrophy 52 Hereditary angioedema HAE 52 Hyperthyroidism 52 obliterative bronchiolitis 52 Moebius syndrome 52 Ankylosing spondylitis 52 drooping eyelid 52 aplastic anemia rare 52 Polycystic Ovary Syndrome 52 Lafora disease 52 toxoplasmosis 52 cystic kidney 52 paralysis blindness 52 dysphasia 52 degenerative spinal 52 fetu 52 Severe Primary IGFD 52 Hypothyroidism 52 syndrome FAS 52 adenomyosis 52 exotropia 52 retinal detachment 52 acetabular dysplasia 52 myoma 52 gastrointestinal stromal tumor 52 microencephaly 52 hyperparathyroidism 52 Gynecomastia 52 Motor neurone disease 52 Pulmonary arterial hypertension 52 thoracic aortic aneurysm 52 autosomal recessive disease 52 Aplastic Anaemia 52 congenital malformations 52 Morton neuroma 52 intra uterine 52 osteochondroma 51 Krabbe disease 51 Benign Paroxysmal Positional Vertigo 51 herpes encephalitis 51 hypophosphatasia 51 Plantar warts 51 Raynaud Syndrome 51 partial amputation 51 infection progressive multifocal 51 monogenic 51 nerve degeneration 51 ischemic bowel 51 torn flexor muscle 51 viral myocarditis 51 broncho pneumonia 51 Avascular Necrosis 51 leiomyomas 51 hyperplastic 51 Pulmonary embolism 51 thrombocytopenia neutropenia 51 Atresia 51 keloid scars 51 CHD7 51 pancreatitis inflammation 51 degenerative muscular 51 neural tube 51 Fallot 51 Gestational diabetes 51 chronic neurological disorder 51 Peripheral neuropathy 51 pheochromocytoma 51 intestinal blockages 51 eosinophilic 51 deafness blindness 51 Charcot foot 51 nephrosis 51 Long QT Syndrome 51 lichen planus 51 Obstructive sleep apnea 51 renovascular hypertension 51 ectopia 51 inguinal hernia 51 kyphosis 51 congenital adrenal hyperplasia 51 brittle bone 51 thyroid dysfunction 51 Nephrogenic Systemic Fibrosis NSF 51 Marfan syndrome 51 arteriovenous malformation 51 dysmotility 51 Polymorphic Ventricular Tachycardia CPVT 51 lymphoblastic lymphoma 51 Sensorineural hearing loss 51 lumbosacral 51 ectopic 51 necrotising enterocolitis 51 defective gene 51 spinal deformities 51 blocked fallopian tubes 51 Spina bifida occurs 51 debilitating affliction 51 Cervical dystonia 51 nephritis 51 arrhythmogenic right 51 Phenylketonuria PKU 51 primitive neuroectodermal tumor 51 Mitochondrial diseases 51 cystic fibrosis hereditary 51 parathyroid glands 51 cardiac hypertrophy 51 laryngeal paralysis 51 facial paralysis 51 fatal neuromuscular disorder 51 endocrine gland 51 degenerative neurological condition 51 Progeria 51 Stargardt Macular Dystrophy 51 mycobacterial infection 51 reflex sympathetic dystrophy 51 Niemann Pick disease 51 nutritional deficiency 51 Idiopathic 51 primary sclerosing cholangitis 51 urogenital chlamydiosis 51 pathologic fracture 51 mitral stenosis 51 leptin deficiency 51 pelvic fractures 51 Duchenne Muscular Dystrophy DMD 51 Alport Syndrome 51 aciduria 51 chronic venous insufficiency 51 healing rib fractures 51 schwannoma 51 Downs Syndrome 51 phthalate syndrome 51 ganglion cysts 51 viral cardiomyopathy 51 genetic defects 51 Tay Sachs Disease 51 muscle spasticity 51 myositis 51 chorioamnionitis 51 disfiguring scars 51 autoinflammatory diseases 51 gastrointestinal GI perforation 51 bicuspid aortic valve 51 fibrodysplasia ossificans progressiva 51 Kufs disease 51 myoclonic epilepsy 51 paraneoplastic 51 metabolic abnormality 51 esotropia 51 Duchenne muscular dystrophy DMD 51 Menkes disease 51 congenital myasthenic syndrome 51 Septicaemia 51 cleft lip 51 polycystic ovarian syndrome 51 recurrent miscarriages 51 fat embolism 51 Fanconi Anaemia 51 primary IGFD 51 spinal meningitis 51 bronchopulmonary dysplasia 51 von Willebrand disease 51 de novo mutations 51 spondylitis 51 intestinal pseudo 51 IUGR 51 NPHP 51 corneal scarring 51 subaortic stenosis 51 plagiocephaly 51 spondylosis 51 Juvenile Rheumatoid Arthritis 51 focal dystonia 51 Wilms Tumour 51 Male pattern baldness 51 generalized dystonia 51 costochondritis 51 Hypertrophic Cardiomyopathy HCM 51 intestinal disorder 51 Morton Neuroma 51 Critical limb ischemia 51 cardiac insufficiency 51 pulmonary hypertension 51 fibular 51 Parasitic twins 51 underactive thyroid gland 51 Eloysa Vasquez 51 immune deficiency 51 pre cancerous lesion 51 omphalocele 51 supratentorial 51 epidural abscess 51 Preeclampsia 51 distended stomach 51 Alopecia Areata 51 cell sarcoma