Related by context. All words. (Click for frequent words.) 68 microcephalic 62 dwarfism 61 achondroplasia 60 microencephaly 60 holoprosencephaly 59 dysmorphic features 59 LB1 58 chromosome abnormality 57 malformations 57 skeletal dysplasia 57 congenital disorder 57 septo optic dysplasia 57 hypoplasia 57 chromosomal abnormality 57 anencephaly 56 H. floresiensis 56 teratoma 56 Marfan syndrome 56 idiopathic 56 dilated cardiomyopathy 56 Apert syndrome 56 dysgenesis 56 #q#.# deletion syndrome 56 infarcts 55 Angelman syndrome 55 hypotonia 55 hypopituitarism 55 Morquio syndrome 55 omphalocele 55 Beckwith Wiedemann syndrome 55 spinocerebellar ataxia 55 spastic diplegia 55 developmental abnormalities 55 microdeletion 55 polydactyly 55 Pervasive Developmental Disorder 55 syringomyelia 55 chromosomal disorder 54 osteogenesis imperfecta 54 neurological abnormalities 54 genetic disorder 54 hyperplastic 54 phthalate syndrome 54 rare chromosomal disorder 54 autosomal recessive 54 situs inversus 54 mental retardation epilepsy 54 hydrops 54 fibrous dysplasia 54 autosomal dominant 54 congenital abnormalities 54 de novo mutations 54 osteopetrosis 54 chromosomal anomaly 54 Hurler syndrome 54 malformation 54 agenesis 54 diaphragmatic hernia 54 Proteus Syndrome 54 congenital abnormality 54 Joubert syndrome 54 Fragile X Syndrome 54 genetically inherited 53 congenital deformity 53 pyloric stenosis 53 neurofibromas 53 Hutchinson Gilford Progeria Syndrome 53 hydrocephaly 53 optic nerve hypoplasia 53 aplasia 53 microcephalics 53 VCFS 53 chromosomal disorders 53 Dwarfism 53 lissencephaly 53 paraganglioma 53 congenital 53 CHARGE syndrome 53 endocasts 53 chromosome deletion 53 Leber congenital amaurosis 53 Dravet syndrome 53 genetic abnormality 53 immunodeficiency 53 primitive neuroectodermal tumors 53 mammillary bodies 53 bone deformities 53 degenerative disorder 53 hemiparesis 53 chromosomal defect 53 cryptorchidism 53 hypoplastic 52 hamartoma 52 neurodevelopmental disorder 52 dyscalculia 52 myelomeningocele 52 persistent pulmonary hypertension 52 skeletal deformities 52 atresia 52 degenerative neurological disorder 52 neurological disorder affecting 52 brain lesions 52 infantile hemangiomas 52 lacunar 52 abnormalities 52 hypertrophic cardiomyopathy HCM 52 dermoid cyst 52 blindness deafness 52 fibrodysplasia ossificans progressiva FOP 52 cerebellar 52 spine curvature 52 Marfan 52 arthrogryposis 52 alpha thalassemia 52 HGPS 52 brain malformation 52 Hutchinson Gilford Progeria 52 Chiari malformation 52 Asperger disorder 52 ectodermal dysplasia 52 Diplodocus 52 meningiomas 52 hominid species 52 RDEB 52 autistic traits 51 Holoprosencephaly 51 spastic cerebral palsy 51 fusiform 51 Klinefelter syndrome 51 cretinism 51 IgA deficiency 51 cerebral infarction 51 corpus callosum 51 Proteus syndrome 51 neurofibromatosis 51 white matter hyperintensities 51 dominantly inherited 51 H. sapiens 51 neurodevelopmental 51 polydactylism 51 osteogenesis imperfecta OI 51 spastic paraplegia 51 congenital disorders 51 Fanconi anemia 51 Ectopia Cordis 51 Lesch Nyhan syndrome 51 neural tube defect 51 chromosome #q#.# [001] 51 rhabdomyosarcoma 51 gene MECP2 51 dyspraxia 51 arthrogryposis multiplex congenita 51 Australopithecus africanus 51 primordial dwarfism 51 primary ciliary dyskinesia 51 craniopagus parasiticus 51 theropod 51 monozygotic twins 51 recessive inheritance 51 ADPKD 51 pulmonary atresia 51 deformity 51 atrial septal defect 51 Hirschsprung disease 51 mosaicism 51 hemiplegia 51 limb deformities 51 tricuspid atresia 51 microcephalin 50 FXTAS 50 polymyalgia rheumatica 50 esophageal atresia 50 Neurofibromatosis type 50 vascular malformation 50 skeletal abnormalities 50 dystrophy 50 proband 50 inherited neurological disorder 50 recessive genetic 50 Joubert Syndrome 50 supratentorial 50 Niemann Pick disease 50 thyroiditis 50 ventricular septal defect 50 genetic defect 50 nonhereditary 50 Arnold Chiari Malformation 50 crania 50 Cerebral palsy 50 structural abnormalities 50 congenital deafness 50 blood clotting disorder 50 aneuploidies 50 Wolf Hirschhorn 50 NF2 50 Prader Willi syndrome 50 brain hemorrhages 50 congenital anomalies 50 fibroma 50 Retinitis pigmentosa 50 Hashimoto thyroiditis 50 neuroblastomas 50 Vitamin B# deficiency 50 myositis 50 Loeys Dietz syndrome 50 hippocampal volumes 50 penetrance 50 behavioral abnormalities 50 diabetes insipidus 50 hamartomas 50 basilar 50 retinal dysfunction 50 paraneoplastic 50 subependymal giant cell 50 sporadic ALS 50 genetic mutation 50 osteochondroma 50 galactosemia 50 Cockayne syndrome 50 cerebral palsy blindness 50 species Australopithecus afarensis 50 bronchopulmonary dysplasia 50 WAGR syndrome 50 DiGeorge syndrome 50 Langerhans cell histiocytosis 50 cerebellar hypoplasia 50 mitochondrial dysfunction 50 dizygotic twins 50 pituitary adenoma 50 Sanfilippo Syndrome 50 Ehlers Danlos syndrome 50 neurofibromatosis type 50 Childhood Disorder 50 congenital diaphragmatic hernia 50 Goldenhar syndrome 50 Hip dysplasia 49 braincase 49 autonomic dysfunction 49 nerve palsy 49 generalized epilepsy 49 Wilms tumor 49 savant syndrome 49 Muscular dystrophy 49 hypertrophic cardiomyopathy 49 highly heritable 49 neurodevelopment disorder 49 Orrorin 49 genetic abnormalities 49 undescended testicles 49 congenital insensitivity 49 beta thalassemia 49 familial adenomatous polyposis FAP 49 neuro developmental disorder 49 imperfecta 49 neuropsychiatric disorder 49 Male pattern baldness 49 Spina bifida 49 enlarged tonsils 49 schwannomas 49 Treacher Collins syndrome 49 osteochondromas 49 neonatal respiratory distress 49 generalized dystonia 49 ataxias 49 undiagnosed celiac disease 49 hypogonadotropic hypogonadism 49 congenital cataract 49 heritable 49 abnormal chromosome 49 childhood disintegrative disorder 49 fibromatosis 49 familial ALS 49 chromosomal anomalies 49 chromosomal alterations 49 Kabuki syndrome 49 Hypoplastic Left Heart 49 kyphosis 49 cortices 49 trisomy 49 polyhydramnios 49 ambiguous genitalia 49 homozygosity 49 McCune Albright 49 autosomal dominant disorder 49 Down syndrome 49 congenital anomaly 49 NF1 49 enterocolitis 49 developmental disorder 49 dysmotility 49 congenital glaucoma 49 apolipoprotein E gene 49 pituitary tumors 49 inherited mutations 49 familial adenomatous polyposis 49 congenital hypothyroidism 49 Congenital 49 chiari malformation 49 Tay Sachs disease 49 torticollis 49 genetic syndromes 49 polycystic ovary syndrome 49 subarachnoid haemorrhage 49 Asberger syndrome 49 carcinoid tumor 49 immunodeficiencies 49 cardiomegaly 49 Sensorineural hearing loss 49 ataxia 49 autism spectrum disorder 49 genetic neuromuscular disorder 49 myotonic dystrophy 49 australopithecines 49 Perthes disease 49 familial clustering 49 hallux valgus 49 auditory neuropathy 49 Becker muscular dystrophy 49 pheochromocytoma 49 Anencephaly 49 peripartum cardiomyopathy 48 developmental delays 48 retinal hemorrhage 48 polycystic kidneys 48 exotropia 48 tuberous sclerosis complex 48 syndromes 48 neoplasm 48 cerebral palsy 48 recurrent miscarriages 48 karyotype 48 velo cardio facial 48 Severe Combined Immunodeficiency 48 #q#.# [002] 48 cerebral palsy epilepsy 48 dyskeratosis congenita 48 MECP2 gene 48 GBA mutations 48 chromosomal abnormalities 48 G#S mutation 48 SRBD 48 IUGR 48 autistic tendencies 48 congenital hydrocephalus 48 myopathies 48 craniopagus 48 tuberous sclerosis 48 thyroid hormone deficiency 48 uterus didelphys 48 chromosomal deletions 48 Retinoblastoma 48 sexually dimorphic 48 FMR1 48 adenomyosis 48 placental mammals 48 cerebri 48 Crouzon Syndrome 48 Usher Syndrome 48 archosaur 48 combined immunodeficiency SCID 48 multisystem disease 48 syndrome FAS 48 Arrhythmogenic Right Ventricular Cardiomyopathy 48 subdural haemorrhage 48 cortical dysplasia 48 australopithecine 48 Klippel Trenaunay Weber 48 Asperger Disorder 48 craniofacial anomalies 48 congenital cataracts 48 periventricular leukomalacia 48 genes predisposing 48 craniofacial 48 Asperger 48 hyperprolactinemia 48 atrophic 48 myelogenous leukemia 48 monogenic 48 Beckwith Wiedemann Syndrome 48 progressive neurodegenerative disorder 48 neurological impairments 48 neuropathology 48 twin transfusion 48 Tourette Syndrome TS 48 Hurler Syndrome 48 intractable epilepsy 48 atrioventricular septal defect 48 Radiographic findings 48 frontotemporal 48 hemangioma 48 Denisovan 48 Tetralogy 48 metabolic abnormalities 48 macrosomia 48 femora 48 Multivariate analyzes 48 Kufs disease 48 Sjögren syndrome 48 neuro degenerative disorder 48 Crouzon syndrome 48 Churg Strauss syndrome 48 CHD7 48 brow ridge 48 Autistic Disorder 48 skeletal malformations 48 gene mutation 48 Li Fraumeni syndrome 48 hypoxic ischemic encephalopathy 48 Anorexia nervosa 48 Cushing syndrome 48 deafness blindness 48 H. erectus 48 autosomal recessive genetic 48 Patau syndrome 48 heterozygous 48 prosopagnosia 48 hereditary deafness 48 Foreign Accent Syndrome 48 hypoplastic left 48 heritability 48 perinatal asphyxia 48 variable immunodeficiency 48 anatomical abnormalities 48 lipoma 48 clumsy gait 48 SNHL 48 #q# [001] 48 autistic spectrum 48 normal karyotype 48 PNET 48 transfusion syndrome 48 Epileptic seizures 48 Wegener granulomatosis 48 acute colitis 48 Osteogenesis imperfecta 47 subclinical hypothyroidism 47 monozygotic twin 47 deformities 47 dermatomyositis 47 Prenatal diagnosis 47 insulin resistance syndrome 47 polycystic ovary syndrome PCOS 47 cardiomyopathies 47 DiGeorge syndrome rare 47 infarctions 47 subdural bleeding 47 untreated celiac disease 47 lymphocytic 47 Hirschsprung Disease 47 asperger syndrome 47 Angelman Syndrome 47 Brugada Syndrome 47 Myotonic dystrophy 47 LVNC 47 birth defect 47 congenital malformation 47 nontraumatic 47 ASDs 47 microvascular disease 47 neurofibroma 47 #p#.# [001] 47 CDH1 47 neurodevelopmental impairment 47 leptin deficiency 47 embryonal rhabdomyosarcoma 47 autosomal recessive disorder 47 lactase deficiency 47 quadriplegic cerebral palsy 47 neurologic symptoms 47 paresis 47 mitochondrial disorders 47 adenoid 47 chromosome abnormalities 47 schwannoma 47 degenerative neurological condition 47 Mental retardation 47 Rubinstein Taybi syndrome 47 curved spine 47 muscle degeneration 47 retinal haemorrhages 47 HNPCC 47 hyperplasia 47 hyperkeratosis 47 #q# deletion 47 medulloblastoma tumors 47 bradykinesia 47 Australopithecus 47 neurological manifestations 47 neurodevelopmental disorders 47 intracerebral 47 hypertrophic 47 ependymoma 47 maxillary 47 autistics 47 hyoid 47 inherited retinal degeneration 47 cardio myopathy 47 mood dysregulation 47 hemophagocytic lymphohistiocytosis 47 Diverticulosis 47 ichthyosis 47 metabolic abnormality 47 LRRK2 gene 47 non syndromic 47 premorbid 47 genetic mutations Spoor 47 idiopathic dilated cardiomyopathy 47 celebral palsy 47 Wilms Tumor 47 Von Willebrand disease 47 genus Homo 47 imperforate anus 47 temporal lobe epilepsy 47 CTEPH 47 gastric carcinoma 47 #q# deletion syndrome 47 Brugada syndrome 47 intraventricular hemorrhage 47 generalized seizures 47 Hemangiomas 47 dissociative disorders 47 systemic amyloidosis 47 fibrodysplasia ossificans progressiva 47 fetu 47 NPHP 47 sirenomelia 47 heterotaxy 47 chromosomal defects 47 Sanfilippo syndrome 47 Moebius syndrome 47 epidermolysis bullosa EB 47 spastic paralysis 47 diffuse intrinsic pontine glioma 47 Fibrous Dysplasia 47 recessive trait 47 Coeliac disease 47 cerebellar ataxia 47 generalized tonic clonic seizures 47 amusia 47 motor neuron degeneration 47 limb malformations 47 PANDAS 47 monotremes 47 autosomal dominant inheritance 47 monoclonal gammopathy 47 disorder ASD 47 posterior fossa 47 periventricular 47 autism Asperger 47 leukoencephalopathy 47 Marfan syndrome genetic 47 benign positional vertigo 47 Primary IGFD 47 hominid 47 Genetic predisposition 47 #q#.# [001] 47 enterovirus infection 47 HLA B# 47 neurological dysfunction 47 Mitochondrial diseases 47 Noonan Syndrome 47 cognitive deficits 47 epididymitis 47 bronchiolitis 47 agnosia 47 disorder FASD 47 mental retardation 47 neurodegenerative disorder 47 habitual snoring 47 chorioamnionitis 47 nerve degeneration 47 optic atrophy 47 Aspergers 47 Klinefelter Syndrome 47 congenital scoliosis 47 cryptogenic stroke 47 underlying pathophysiology 47 retinal hemorrhages 47 floresiensis 47 truncus arteriosus 47 Homo erectus 47 chordates 47 Hypophosphatasia 47 lysosomal storage diseases 47 phonic tics 47 testicular tumors 47 sCJD 47 homozygous FH 47 hirsutism 47 Dilated cardiomyopathy 47 FSGS 47 cryptogenic 47 nonsense mutation 47 lung lesions 47 spastic quadriplegia 47 congenital malformations 47 incurable neurological disorder 47 Hypertrophic 47 klotho 47 Paranthropus boisei 47 Shy Drager syndrome 47 parkinsonism 47 calculi 47 polyneuropathy 47 atherosclerotic lesions 47 Hutchinson Gilford progeria 47 APOE gene 47 nonalcoholic cirrhosis 47 leukodystrophy 46 monozygotic 46 amenorrhoea 46 polycystic 46 juvenile myelomonocytic leukemia 46 static encephalopathy 46 idiopathic epilepsy 46 Dromomeron 46 dysplasia 46 polymyositis 46 post transplant lymphoproliferative 46 Langerhans Cell Histiocytosis 46 cystic fibrosis chronic pancreatitis 46 autoimmune encephalitis 46 Birth defects 46 genital abnormalities 46 spinal muscle atrophy 46 Epidermolysis bullosa 46 tracheal stenosis 46 neurological 46 arrhythmogenic right 46 epilepsies 46 H. habilis 46 ataxia telangiectasia 46 Tourette syndrome neurological disorder 46 ramidus 46 dizygotic 46 Rett syndrome 46 androgenetic alopecia 46 chromosomal imbalance 46 involuntary tics 46 unknown etiology 46 Wernicke Korsakoff syndrome 46 born prematurely 46 Psittacosaurus 46 Aicardi syndrome 46 mental retardation blindness 46 DiGeorge Syndrome 46 cardiomyopathy 46 Osteogenesis Imperfecta 46 Down syndrome autism 46 sacral agenesis 46 hormonal disorder 46 Eisenmenger syndrome 46 AAT deficiency 46 hormonal abnormalities 46 frameshift mutation 46 fat embolism 46 ocular albinism 46 associated tremor ataxia 46 aniridia 46 granulomas 46 chromosomal rearrangements 46 nonischemic 46 meningeal 46 autism cerebral palsy 46 Marfan Syndrome 46 sensorineural hearing loss 46 poorer prognosis 46 neuritis 46 enzyme deficiency 46 stress cardiomyopathy 46 morphologic 46 Mendelian disorders 46 pyelonephritis 46 lateral ventricles 46 neurodevelopmental disability 46 Archaeopteryx 46 testicular descent 46 Asperger syndrome milder 46 petit mal seizures 46 adenoma 46 FMR1 gene 46 retinitis pigmentosa RP 46 blastomeres 46 combined immunodeficiency 46 eosinophilic 46 Medulloblastoma 46 CNTNAP2 46 serum IGF 46 limb girdle muscular dystrophy 46 stooped posture 46 incurable genetic 46 PON1 46 microtia 46 lipomas 46 pulmonary hypoplasia 46 narcolepsy cataplexy 46 congential 46 Mycoplasma pneumoniae 46 fatal neuromuscular disorder 46 premalignant 46 hominoids 46 congenital brain tumor 46 Wilm tumor 46 connective tissue disorder 46 clinically insignificant 46 recessively inherited 46 intercranial 46 neuroblastoma tumor 46 craniosynostosis 46 vertebral artery dissection 46 cerebral atrophy 46 cystic hygroma 46 neonatal encephalopathy 46 cyanosis 46 bilaterians 46 extreme prematurity 46 neurobiological disorder 46 tyrannosaurids 46 cardiac hypertrophy 46 epidermolysis bullosa 46 Dysplasia 46 Rh incompatibility 46 primitive neuroectodermal tumor 46 C#Y 46 progeria rare 46 left ventricular systolic 46 karyotypes 46 idiopathic generalized epilepsy 46 eosinophilic esophagitis 46 recessive gene 46 leiomyomas 46 mild cognitive 46 Pierolapithecus 46 anterior temporal 46 aY chromosome 46 euthymic patients 46 juvenile idiopathic arthritis JIA 46 acute subdural hematoma 46 hyperinsulinism 46 immunodeficiency disorder 46 fallot 46 recurrent abdominal pain 46 chronic idiopathic 46 precocious puberty 46 polycystic ovarian syndrome PCOS 46 uterine tumors 46 FASPS 46 Homo genus 46 acetabular dysplasia 46 hematological abnormalities 46 polymorphic ventricular tachycardia 46 neuropathological 46 Obsessive compulsive disorder 46 Leber hereditary optic neuropathy 46 Down syndrome chromosomal disorder 46 acute myocarditis 46 autoinflammatory diseases 46 anhidrosis 46 cognitive dysfunction 46 SCA5 46 rCBF 46 autistic regression 46 mtDNA mutations 46 underactive thyroid gland 46 Rhabdomyosarcoma 46 recurrent laryngeal nerve 46 Insulin resistance 46 prenatally diagnosed 46 hereditary disorder 46 inherited genetic mutations 46 hypertrichosis 46 degenerative neurological disease 46 Chiari Malformation 46 histiocytosis 46 autism neurological disorder 46 Paranthropus 46 Pelizaeus Merzbacher disease 46 syndrome FXTAS 46 mitral valve regurgitation 46 Sturge Weber syndrome 46 grand mal 46 SHANK3 46 internalizing disorders 46 orchitis 46 Lafora disease 46 neurological sequelae 46 Massospondylus 46 apelike 46 left ventricular hypertrophy 46 familial hypercholesterolemia 46 myotonic 46 neurodevelopmental disorder characterized 46 proximal colon 46 hemochromatosis 46 spleen liver 46 cerebral ischemia 46 phenotypes 46 premature ovarian 46 dissociative amnesia 46 myocarditis 46 encephalitis meningitis 46 Uterine fibroids 46 developmental disorders 46 APOE ε4 46 systemic scleroderma 46 amniotic fluid embolism 46 ischemic lesions 46 Sleep disordered breathing 46 heterozygotes 46 HMGA2 46 mitochondrial disorder 46 congenital adrenal hyperplasia CAH 46 Apert Syndrome 46 Obstructive sleep apnea 46 hippocampal volume 46 Duchene muscular dystrophy 46 autosomal dominant polycystic kidney 46 aortic annulus 46 Inkayacu 46 neurological disorder 46 microangiopathy 46 chondrosarcoma 46 dysgraphia 45 Erb palsy 45 p# mutations 45 Australopithecines 45 granulomatous 45 tic disorder 45 tertiary syphilis 45 neuromotor 45 Henoch purpura 45 familial aggregation 45 roseola 45 polycystic ovaries 45 polypoid 45 Krabbe Leukodystrophy 45 Acanthostega 45 juvenile idiopathic arthritis 45 choriocarcinoma 45 cystic lesions 45 forelimbs 45 Hypertrophic cardiomyopathy 45 Leber congenital amaurosis LCA 45 presbycusis 45 neoplasms 45 Y chromosomal 45 cerebal palsy 45 extrapyramidal symptoms 45 Severe Primary IGFD 45 diverticulum 45 dysplastic 45 ptosis 45 hippocampal atrophy 45 predisposing factor 45 laterality 45 genetic mutations 45 retinitis pigmentosa hereditary 45 bladder exstrophy 45 Leydig cell 45 severely deformed 45 ANCA associated 45 pathophysiologic 45 curved spines 45 nonmalignant 45 deafness neurological 45 Pulmonary hypertension 45 neonate 45 ARVD 45 gene variants 45 Aplastic anemia 45 subcortical 45 enamel defects 45 Fragile X syndrome 45 Bardet Biedl syndrome 45 neurological disorder characterized 45 prefrontal regions 45 disorders FASD 45 otitis media 45 hereditary spastic paraplegia 45 cervical spine fractures 45 haemorrhagic 45 Ebstein anomaly 45 Peutz Jeghers syndrome 45 Tuberous Sclerosis Complex 45 polycystic disease 45 Long QT syndrome 45 hypothalamic hamartoma 45 shorter telomeres 45 mild mental retardation 45 Bedbug bites 45 optic nerve sheath 45 EoE 45 disorders ASD 45 IGF1 45 congenital birth defects 45 neurological impairment 45 mammary tumors 45 azoospermia 45 malignant neoplasm 45 aneuploidy 45 osteochondrosis 45 fatal neurodegenerative 45 interrupted aortic arch 45 nuchal 45 Migraine headaches 45 myeloproliferative neoplasms 45 spinal bifida 45 infantile onset 45 phenotypically 45 craniofacial defects 45 muscle rigidity 45 neurotypical 45 Fragile X gene 45 intestinal ulcers 45 compulsive hoarding 45 serotonin defects 45 undescended 45 Polycystic ovary syndrome 45 glomerulonephritis 45 tunica vaginalis 45 radiographic findings 45 tics involuntary 45 Dravet Syndrome 45 Loeys Dietz 45 neurologic disorders 45 hereditary hemorrhagic telangiectasia 45 Protoceratops 45 retinal blastoma 45 brachial plexus palsy 45 Gynecomastia 45 aciduria 45 MEN 2B 45 hemorrhagic colitis 45 neurosensory 45 profound deafness 45 chordate 45 rheumatic disease 45 Oppositional Defiant Disorder 45 Eloysa Vasquez 45 gyri 45 nongenetic 45 chronicity 45 pathognomonic 45 Chronic fatigue 45 Diamond Blackfan anemia 45 cysts 45 parkinsonian 45 DISC1 gene 45 subclinical hyperthyroidism 45 idiopathic cardiomyopathy 45 anosognosia 45 Parkinson disease degenerative 45 homozygous familial hypercholesterolemia 45 atrophic gastritis 45 hyperactivity impulsivity 45 ventricular dilation 45 shortened telomeres 45 neuritic 45 cystic 45 CdLS 45 ceroid lipofuscinosis NCL 45 vascular dysfunction 45 hypercalcaemia 45 Asperger syndrome mild 45 neurologic complications 45 Cystic fibrosis CF 45 pediatric cataract 45 AAT Deficiency 45 hip dysplasia 45 skeletal fluorosis 45 genetic lysosomal storage 45 β thalassemia 45 Usher syndrome 45 MYCN amplification 45 paragangliomas 45 GH deficiency 45 bulbar 45 venous malformation 45 Heterodontosaurus 45 ganglion 45 disordered breathing 45 arthrosis 45 Goldenhar Syndrome 45 tumoral 45 ventricular cardiomyopathy 45 craniofacial deformities 45 impaired cognition 45 myostatin gene 45 infantile spasms 45 primary pulmonary hypertension 45 hypoxia ischemia 45 lactose malabsorption 45 monophyletic 45 axonal damage 45 craniofacial duplication 45 alexia 45 motor neuropathy 45 haemorrhages 45 trabecular bone