Related by context. All words. (Click for frequent words.) 68 achondroplasia 62 primordial dwarfism 62 microcephaly 59 skeletal dysplasia 58 neurofibromatosis 58 genetic disorder 57 osteogenesis imperfecta 56 Dwarfism 56 spastic diplegia 56 chromosomal disorder 55 Fragile X Syndrome 55 congenital disorder 55 septo optic dysplasia 54 Marfan syndrome 54 spina bifida 54 cerebral palsy 54 Proteus syndrome 54 birth defect 53 Angelman Syndrome 53 Fanconi anemia 53 Joubert Syndrome 52 Proteus Syndrome 52 mitochondrial disease 52 scoliosis 52 arthrogryposis 52 deformity 52 degenerative disorder 52 optic nerve hypoplasia 52 Angelman syndrome 52 muscular dystrophy 52 Down syndrome 52 chromosomal abnormality 52 Niemann Pick disease 51 Chiari malformation 51 Muscular dystrophy 51 osteogenesis imperfecta OI 51 holoprosencephaly 51 Aicardi syndrome 51 Tourette syndrome 51 Cerebral palsy 51 rare chromosomal disorder 51 savant syndrome 51 Hutchinson Gilford Progeria Syndrome 51 sacral agenesis 50 degenerative neurological disorder 50 brittle bone 50 Joubert syndrome 50 Goldenhar syndrome 50 Klinefelter syndrome 50 Tourette 50 Sanfilippo syndrome 50 rhabdomyosarcoma 50 chromosome abnormality 50 degenerative muscular 50 arthrogryposis multiplex congenita 50 Pompe Disease 50 genetically inherited 50 genetic abnormality 50 ectodermal dysplasia 50 Beckwith Wiedemann Syndrome 49 CdLS 49 Asperger syndrome 49 Marfan 49 epidermolysis bullosa EB 49 Rubinstein Taybi syndrome 49 Dravet syndrome 49 congenital 49 Apert syndrome 49 spastic cerebral palsy 49 albinism 49 NF2 49 tuberous sclerosis 49 chiari malformation 49 brain malformation 49 Fragile X syndrome 49 Osteogenesis Imperfecta 49 hip dysplasia 49 Hurler syndrome 49 Asperger Syndrome mild 49 Spina bifida 49 Wilms tumor 49 microencephaly 49 Pervasive Developmental Disorder 49 Apert Syndrome 49 malformation 49 Marfan Syndrome 49 motor neuron disease 49 polycystic ovary syndrome 49 inherited retinal degeneration 48 genetic defect 48 Pompe disease rare 48 spinocerebellar ataxia 48 neurological disorder 48 Morquio syndrome 48 Obsessive compulsive disorder 48 Hirschsprung disease 48 CHARGE syndrome 48 spinal muscular atrophy 48 metabolic disorder 48 Hutchinson Gilford Progeria 48 Angelman 48 Leber congenital amaurosis 48 idiopathic 48 degenerative 48 incurable genetic 48 diaphragmatic hernia 48 alopecia 48 polydactyly 48 Asperger Disorder 48 polycystic ovarian syndrome 48 Shwachman Diamond Syndrome 48 chromosomal defect 48 myotonic dystrophy 48 DiGeorge syndrome 48 teratoma 48 Crouzon Syndrome 48 Dravet Syndrome 48 mitochondrial disorder 47 Asberger syndrome 47 Retinitis pigmentosa 47 dilated cardiomyopathy 47 mosaicism 47 bone deformities 47 Cockayne syndrome 47 Hurler Syndrome 47 cerebal palsy 47 neurodevelopmental disorder 47 anencephaly 47 Wilms Tumor 47 Beckwith Wiedemann syndrome 47 Hashimoto thyroiditis 47 juvenile rheumatoid arthritis 47 Neurofibromatosis 47 chromosome deletion 47 dyscalculia 47 developmental disorder 47 polycystic kidney disease 47 genetic syndromes 47 static encephalopathy 47 Ehlers Danlos syndrome 47 autism 47 Hirschsprung Disease 47 Asperger disorder 47 Eloysa Vasquez 47 Treacher Collins Syndrome 47 hereditary disorder 47 Sanfilippo Syndrome 47 cerebellar ataxia 47 Asperger 47 degenerative nerve disorder 47 congenital heart 47 Progeria 46 Noonan Syndrome 46 hypertrichosis 46 dyskeratosis congenita 46 dyspraxia 46 ceroid lipofuscinosis NCL 46 autosomal recessive 46 Usher Syndrome 46 skeletal abnormalities 46 recessive genetic 46 recessive trait 46 autistic tendencies 46 DiGeorge Syndrome 46 hemangioma 46 ambiguous genitalia 46 autism spectrum disorder 46 neurofibroma 46 Prader Willi syndrome 46 intersex 46 hereditary deafness 46 uterus didelphys 46 malformations 46 sirenomelia 46 epidermolysis bullosa 46 phthalate syndrome 46 leukodystrophy 46 Gynecomastia 46 myositis 46 Osteosarcoma 46 deformities 46 neurofibromas 46 quadriplegic cerebral palsy 46 chromosomal anomaly 46 cryptorchidism 46 incurable neurological disorder 46 ichthyosis 46 Retinoblastoma 46 Aspergers syndrome 46 Klinefelter Syndrome 46 precocious puberty 46 Male pattern baldness 46 Down syndrome chromosomal disorder 46 Treacher Collins syndrome 46 Aspergers Syndrome 46 polydactylism 46 Li Fraumeni syndrome 46 dysplasia 46 Tay Sachs disease 46 ataxia 46 NF1 46 Maroteaux Lamy syndrome 46 neurological disorder affecting 45 Medulloblastoma 45 onset diabetes 45 syringomyelia 45 imperfecta 45 ataxia telangiectasia 45 Tourette syndrome neurological disorder 45 Downs Syndrome 45 myotonic 45 autism neurological disorder 45 eosinophilic esophagitis 45 Rhabdomyosarcoma 45 autosomal dominant 45 Chiari Malformation 45 Attention Deficit Disorder ADD 45 hereditary spastic paraplegia 45 clubfoot 45 fibrous dysplasia 45 congenital diaphragmatic hernia 45 neurobiological disorder 45 Pelizaeus Merzbacher disease 45 Leber congenital amaurosis LCA 45 dystonia 45 WAGR syndrome 45 gynecomastia 45 progeria 45 polycystic ovaries 45 neurofibromatosis NF 45 congenital deformity 45 lissencephaly 45 Hip dysplasia 45 dystrophy 45 Treacher Collins 45 Erb palsy 45 inherited neurological disorder 45 Goldenhar Syndrome 45 retinitis pigmentosa 45 Diamond Blackfan anemia 45 degenerative disease 45 congenital hydrocephalus 45 epilepsy 45 Battens Disease 45 spastic paraplegia 45 ADPKD 45 transsexualism 45 kyphosis 45 Sturge Weber 45 hormonal disorder 45 McCune Albright 45 gene mutation 45 Anorexia nervosa 45 Becker muscular dystrophy 45 sickle cell anemia 45 congenital insensitivity 45 VCFS 45 craniopagus parasiticus 45 esophageal atresia 45 dyslexia 45 polycystic ovarian syndrome PCOS 45 developmental abnormalities 45 cerebellar hypoplasia 45 dysmorphic features 45 paraplegia 45 Congenital Adrenal Hyperplasia 45 prosopagnosia 45 corneal dystrophy 45 Maroteaux Lamy Syndrome 45 limb girdle muscular dystrophy 45 primary ciliary dyskinesia 45 fatal neurodegenerative 45 mental retardation 45 aciduria 44 Lafora disease 44 Foreign Accent Syndrome 44 spinal bifida 44 Von Willebrand disease 44 acromegaly 44 intractable epilepsy 44 connective tissue disorder 44 Polycystic ovary syndrome 44 vascular malformation 44 hereditary disorders 44 HGPS 44 congenital abnormality 44 dermatomyositis 44 aneuploidies 44 Spina Bifida 44 Stargardt disease 44 Tourette Syndrome 44 Apert 44 hereditary blindness 44 blindness deafness 44 congenital cataracts 44 neurofibromatosis genetic disorder 44 skeletal deformities 44 neuromuscular disorder 44 compulsive hoarding 44 Wegener granulomatosis 44 pyloric stenosis 44 pulmonary atresia 44 kidney disease 44 neurodegenerative disorder 44 Pompe disease 44 celebral palsy 44 familial adenomatous polyposis 44 Psoriatic arthritis 44 congenital glaucoma 44 retinal dysfunction 44 Niemann Pick 44 Asperger Syndrome 44 hypoplasia 44 congenital muscular dystrophy 44 Perthes disease 44 peripartum cardiomyopathy 44 Asperger syndrome mild 44 autism spectrum disorders 44 #q#.# deletion syndrome 44 Duchenne muscular dystrophy 44 enzyme deficiency 44 chromosomal disorders 44 ocular albinism 44 craniosynostosis 44 Arthrogryposis 44 deafness 44 juvenile diabetes 44 Crigler Najjar syndrome 44 neurofibromatosis type 44 rheumatic disease 44 hypertrophic cardiomyopathy HCM 44 spastic paralysis 44 Crouzon syndrome 44 gender dysphoria 44 Autism Spectrum Disorder 44 achromatopsia 43 blood clotting disorder 43 mitochondrial myopathy 43 cerebral palsy epilepsy 43 pattern baldness 43 diabetes 43 Leber Congenital Amaurosis LCA 43 rhabdomyosarcoma rare 43 neuroblastoma 43 Porphyria 43 degenerative neuromuscular disease 43 histiocytosis 43 recessive gene 43 scoliosis curvature 43 Kenadie 43 juvenile myelomonocytic leukemia 43 neuromuscular disease 43 torticollis 43 body dysmorphic disorder 43 Fanconi Anaemia 43 Spinal muscular atrophy 43 underactive thyroid 43 cardiomyopathy 43 neuropsychiatric disorder 43 Osgood Schlatter disease 43 insulitis 43 dystonia neurological movement 43 congenital kidney 43 atresia 43 tuberous sclerosis complex 43 paraganglioma 43 cretinism 43 dominantly inherited 43 FSGS 43 combined immunodeficiency 43 AAT deficiency 43 phenylketonuria 43 Fanconi anemia rare 43 adrenal cancer 43 velo cardio facial 43 growth hormone deficiency 43 genetic disorders 43 Aplastic anemia 43 trisomy 43 craniofacial 43 Rett syndrome 43 Sandhoff disease 43 lymphoblastic lymphoma 43 Rett Syndrome 43 Attention Deficit Hyperactive Disorder 43 polymyalgia 43 Tetralogy 43 hypotonia 43 Henoch purpura 43 genetic mutations 43 anorexia nervosa 43 progeria rare 43 Duchene muscular dystrophy 43 bronchopulmonary dysplasia 43 fatal neurodegenerative disorder 43 FXTAS 43 disease 43 Moebius Syndrome 43 muscle degeneration 43 Syndrome SADS 43 DiGeorge syndrome rare 43 biliary atresia 43 Brugada Syndrome 43 hydrocephalus 43 alopecia areata 43 body dysmorphic 43 Krabbe Leukodystrophy 43 Hypoplastic Left Heart 43 Hutchinson Gilford progeria 43 undiagnosed celiac disease 43 asperger syndrome 43 retinitis pigmentosa RP 43 Diverticulosis 43 osteosarcoma bone 43 congenital abnormalities 43 autism Asperger 43 congenital adrenal hyperplasia CAH 43 mammary tumors 43 abnormal chromosome 43 embryonal rhabdomyosarcoma 43 Parkinson's 43 congenital amputation 43 congenital malformation 42 RDEB 42 Asberger Syndrome 42 genetic mutation 42 paraneoplastic 42 blastoma 42 retinitis pigmentosa hereditary 42 abnormalities 42 quadriplegia 42 immunodeficiency disorder 42 heterotaxy 42 curved spine 42 fatal neuromuscular disorder 42 de novo mutations 42 infantile hemangiomas 42 limb deformities 42 Scoliosis 42 Cystic fibrosis CF 42 invasive secretory carcinoma 42 neural tube defect 42 systemic scleroderma 42 hypertrophic cardiomyopathy 42 incurable neurodegenerative disease 42 genetic abnormalities 42 Gaucher disease 42 Down Syndrome 42 Dysplasia 42 Langerhans cell histiocytosis 42 galactosemia 42 Osteogenesis imperfecta 42 Coeliac disease 42 MCAD deficiency 42 AAT Deficiency 42 spastic quadriplegic cerebral palsy 42 congenital adrenal hyperplasia 42 neuro developmental disorder 42 Sturge Weber syndrome 42 Cystic fibrosis 42 nonalcoholic cirrhosis 42 neuroblastoma tumor 42 disorder FASD 42 vasculitis 42 lysosomal storage diseases 42 Rett syndrome neurological disorder 42 cystic fibrosis 42 autism spectrum 42 Atopic dermatitis 42 Fibrous Dysplasia 42 Motor neurone disease 42 sporadic ALS 42 congenital anomaly 42 Autism Spectrum Disorder ASD 42 Aspergers 42 retinoblastoma 42 truncus arteriosus 42 progressive neurodegenerative disorder 42 dermoid cyst 42 severely deformed 42 cardio myopathy 42 subependymal giant cell 42 chromosomal abnormalities 42 Ewings Sarcoma 42 Congenital 42 neurodevelopment disorder 42 Syndrome 42 autism dyslexia 42 Kufs disease 42 hereditary diseases 42 developmental disorders 42 Massospondylus 42 granulomas 42 recessive inheritance 42 Myotonic dystrophy 42 hypophosphatasia 42 psychosocial dwarfism 42 Rhabdomyosarcoma rare 42 HIBM 42 Lesch Nyhan syndrome 42 autism cerebral palsy 42 Body Dysmorphic Disorder BDD 42 verbal apraxia 42 microvascular angina 42 bladder exstrophy 42 aplastic anemia 42 obsessive compulsive disorder OCD 42 primordial dwarf 42 Tuberous Sclerosis Complex 42 dysgenesis 42 Aicardi Syndrome 42 hypoplastic left 42 Binge eating 42 Uterine fibroids 42 retinal degeneration 42 chromosomal defects 42 Tourette Syndrome TS 42 adrenoleukodystrophy ALD 42 hamartoma 42 profound deafness 42 variable immunodeficiency 42 osteopetrosis 42 mental retardation epilepsy 42 congenital disorders 42 dysautonomia 42 Parkinson degenerative 42 mitochondrial dysfunction 42 FTLD 42 congenital brain tumor 42 Histiocytosis 42 hyperemesis gravidarum 42 Prader Willi Syndrome 42 Mitochondrial disease 42 gestational diabetes 42 developmental delays 42 Charcot Marie Tooth 42 Periodontal disease 42 hemophagocytic lymphohistiocytosis 42 inherited neurodegenerative disorder 42 recurrent miscarriages 41 immunodeficiency 41 Asperger syndrome milder 41 Duchenne 41 fibrodysplasia ossificans progressiva FOP 41 enlarged tonsils 41 cysts 41 bipolar illness 41 degenerative neurological disease 41 childhood leukemia 41 congenital hypothyroidism 41 manic depression bipolar disorder 41 Fragile X gene 41 puerperal psychosis 41 childhood disintegrative disorder 41 plagiocephaly 41 syndromes 41 Holoprosencephaly 41 lysosomal diseases 41 biliary atresia rare 41 PKU genetic 41 polycystic kidneys 41 cerebral palsy neurological disorder 41 craniopagus 41 congenital blindness 41 synovial sarcoma 41 Polycystic kidney disease 41 ASDs 41 Vitamin B# deficiency 41 Ewing sarcoma bone 41 PDD NOS 41 inherited neurodegenerative 41 neuro muscular disorder 41 autosomal recessive genetic 41 retinoblastoma rare 41 aniridia 41 clubfeet 41 Transverse Myelitis 41 polymyalgia rheumatica 41 congenital deafness 41 mitochondrial diseases 41 primitive neuroectodermal tumors 41 Loeys Dietz syndrome 41 hemochromatosis 41 cystic hygroma 41 immunodeficiencies 41 paruresis 41 Spinal Muscular Atrophy 41 familial ALS 41 dissociative amnesia 41 lymphoblastic leukemia 41 Persistent Sexual Arousal 41 Epidermolysis bullosa 41 medium chain acyl 41 reactive attachment 41 Severe Primary IGFD 41 osteochondroma 41 spinal muscular atrophy SMA 41 hereditary degenerative 41 neurogenetic 41 Overactive bladder 41 rare neurological disorder 41 infantile spasms 41 inflammatory bowel disease 41 deformed limbs 41 Ichthyosis 41 facial deformity 41 fibromatosis 41 omphalocele 41 Vertebral fractures 41 Alopecia Areata 41 Mermaid Syndrome 41 Alport Syndrome 41 Retinitis Pigmentosa RP 41 Fanconi Anemia 41 arthritis 41 neuro degenerative disorder 41 Wilm tumor 41 Biliary atresia 41 cerebri 41 syndrome 41 alzheimer disease 41 neurodevelopmental 41 abnormal curvature 41 dowager hump 41 Savant Syndrome 41 Autism Spectrum 41 agenesis 41 migraine aura 41 bony growths 41 progressive neurodegenerative disease 41 Marfan syndrome genetic 41 muscular dystrophy cystic fibrosis 41 frontal temporal dementia 41 mitochondrial disorders 41 folate deficiency 41 moyamoya 41 bicuspid aortic valve 41 abnormality 41 androgenetic alopecia 41 Down syndrome autism 41 pulmonary stenosis 41 obsessive compulsive disorder 41 autoimmune disorder 41 goiter 41 alpha thalassemia 41 polycystic ovary syndrome PCOS 41 medulloblastoma malignant brain tumor 41 dissociative disorders 41 generalized epilepsy 41 Fanconi 41 Obsessive Compulsive Disorder OCD 41 neurodegenerative disease 41 Combined Immune Deficiency 41 spasmodic dysphonia 41 idiopathic epilepsy 41 giant danio 41 nephrotic syndrome 41 Peutz Jeghers syndrome 41 genetic defects 41 leukemia 41 sickle cell disease 41 TTTS 41 congential 41 beta thalassemia 41 manic depressive disorder 41 fetu 41 retrograde amnesia 41 Duchenne Muscular Dystrophy 41 genetic lysosomal storage 41 Diffuse Intrinsic Pontine Glioma 41 intersexuality 41 leukoencephalopathy 41 streptococcus infection 41 diffuse pontine glioma 41 auditory neuropathy 41 Cushing syndrome 41 Hydrocephalus 41 disorder 41 myoclonic epilepsy 41 infarcts 41 Lou Gehrigs disease 41 cyclic vomiting syndrome 41 chronic autoimmune disorder 41 anhidrosis 41 FSHD 40 bi polar disorder 40 Moebius syndrome 40 Lennox Gastaut syndrome 40 Severe Combined Immunodeficiency 40 Bardet Biedl syndrome 40 Gestational diabetes 40 alveolar rhabdomyosarcoma 40 hereditary hemorrhagic telangiectasia 40 Dystonia 40 situs inversus 40 enlarged breasts 40 spinal curvature 40 intellectual disability 40 idiopathic scoliosis 40 Crohn disease chronic 40 inbreeding depression 40 neurodevelopmental disorders 40 long QT syndrome 40 spastic quadriplegia 40 Alport syndrome 40 Arnold Chiari Malformation 40 spine curvature 40 insulin resistance syndrome 40 hepatoblastoma 40 1 diabetes T1D 40 Parkinson disease neurological disorder 40 gynaecomastia 40 microdeletion 40 Morquio Syndrome 40 Ectodermal Dysplasia 40 neuroblastomas 40 congenital scoliosis 40 obsessive compulsive behaviors 40 hypothyroidism 40 congenital cataract 40 prion disease 40 fatty liver disease 40 persistent pulmonary hypertension 40 apraxia 40 diverticulosis 40 myelomeningocele 40 Wolf Hirschhorn 40 Primary IGFD 40 genetic neuromuscular disorder 40 juvenile dermatomyositis 40 Kawasaki Disease 40 amniotic fluid embolism 40 microcephalics 40 autosomal dominant polycystic kidney 40 Guillain Barre Syndrome 40 autistic spectrum 40 onset Alzheimer 40 hydrops 40 Wilm Tumor 40 autistic traits 40 Irritable bowel syndrome IBS 40 hydrocephaly 40 disordered eating 40 Amyotrophic lateral sclerosis ALS 40 Stargardt Macular Dystrophy SMD 40 Juvenile Rheumatoid Arthritis 40 debilitating neurological disorder 40 craniofacial defects 40 Klippel Trenaunay Weber 40 hormone deficiency 40 bipolar disorder 40 Fragile X 40 vascular anomalies 40 syndrome FXTAS 40 inherited degenerative 40 osteopenia 40 body dysmorphia 40 Varicose veins 40 disease NAFLD 40 mutated gene 40 epileptic seizures 40 fibrodysplasia ossificans progressiva 40 Marfan syndrome connective tissue 40 cystic fibrosis hereditary 40 IDDM 40 Chronic sinusitis 40 diffuse intrinsic pontine glioma 40 Neurofibromatosis type 40 CHD7 40 trichotillomania 40 Sturge Weber Syndrome 40 associated tremor ataxia 40 cerebral palsey 40 primary biliary cirrhosis 40 male reproductive organs 40 Adrenoleukodystrophy 40 retinal blastoma 40 progressive neurological disorder 40 carbohydrate intolerance 40 Krabbe leukodystrophy 40 Peanut allergy 40 Asperger Syndrome AS 40 Parasitic twins 40 Leber Congenital Amaurosis 40 Stargardt Macular Dystrophy 40 muscle dysmorphia 40 Bacterial vaginosis 40 Myopathy 40 arachnoiditis 40 gastroschisis 40 autoimmune disease 40 degenerative retinal disease 40 endocrine disorder 40 lactase deficiency 40 Rh incompatibility 40 Xeroderma Pigmentosum XP 40 catatonic schizophrenia 40 calcium deficiency 40 multisystem disorder 40 arteriovenous malformation 40 developmental disability 40 hirsutism 40 rickets 40 Postnatal depression 40 proximal femoral focal 40 ADHD 40 Attention Deficit Disorder 40 molybdenum cofactor deficiency 40 Childhood Disorder 40 bipolar affective disorder 40 optic atrophy 40 Fetal Alcohol Syndrome 40 late infantile neuronal 40 primary pulmonary hypertension 40 inherited mutations 40 orthostatic intolerance 40 progressive degenerative neurological 40 pontine glioma 40 neural tube defects NTDs 40 retinopathy 40 mental illness 40 schizophrenia 40 Burkitt lymphoma 40 genetic mutations Spoor 40 autism spectrum disorders ASDs 40 metachromatic leukodystrophy 40 Endometrial cancer 40 Bipolar disorder 40 dermopathy 40 male infertility 40 monozygotic twins 40 polycystic disease 40 autoimmune encephalitis 40 lymphocytic leukemia 40 reactive arthritis 40 Ewing sarcoma rare 40 spinal muscle atrophy 40 dermoid 40 amenorrhea 40 factitious disorder 40 ADA SCID 40 undescended testicles 40 metabolic abnormality 40 Iron deficiency anemia 40 Hypothyroidism 40 hind limbs 40 non syndromic 40 nongenetic 40 Usher syndrome 40 hyperplasia 40 reflex sympathetic dystrophy 40 cataracts 40 spina bifida defect 40 Alopecia 40 pannus 40 aneuploidy 39 Normal Pressure Hydrocephalus 39 bunions 39 incurable neurological disease 39 cystic fibrosis CF 39 Sever Disease 39 myasthenia gravis 39 recessively inherited 39 dimentia 39 cranial facial 39 Insulin resistance 39 myopathy 39 spina bifida birth 39 Ataxia 39 muscle wasting 39 Myasthenia gravis 39 epididymitis 39 Ewing sarcoma 39 mental retardation syndromes 39 elephantiasis 39 genital abnormalities 39 Postpartum psychosis 39 Krabbe disease 39 thyroiditis 39 celiac disease 39 Wilms tumors 39 Ankylosing spondylitis 39 brachial plexus palsy 39 osteoarthritis degenerative 39 G#S mutation 39 undiagnosed sleep apnea 39 genital deformities 39 fibroma 39 Hemochromatosis 39 MPGN 39 Oppositional Defiant Disorder 39 Moyamoya disease 39 arthritis RA 39 chiari 39 premature birth 39 coprolalia 39 Myocarditis 39 Parkinsons 39 lactose malabsorption 39 multiple endocrine neoplasia 39 presbycusis 39 aortic dissection 39 preeclampsia 39 progressive degenerative 39 Bi Polar Disorder 39 visual impairment 39 unprovoked seizures 39 Retinopathy 39 Hyperthyroidism 39 rare autosomal recessive 39 nutritional deficiency 39 disc degeneration 39 lysosomal storage disease 39 paresis 39 Alzeheimer 39 Reactive Attachment Disorder 39 muscular dystrophies 39 benign tumors 39 dyslexia dyspraxia 39 primary ovarian insufficiency 39 congenital birth defects 39 Polycystic Ovary Syndrome 39 hemangiomas 39 Duchenne Muscular Dystrophy DMD 39 stooped posture 39 choriocarcinoma 39 hemolytic anemia 39 eating disorder 39 Churg Strauss syndrome 39 incidentalomas 39 MCADD 39 DIPG 39 sarcopenia 39 Trisomy 39 infertility 39 morbidly obese 39 degenerative nerve disease 39 noncancerous tumors 39 spinal chord injuries 39 neonatal respiratory distress 39 Hemangiomas 39 aspergers syndrome 39 hyperplastic 39 histrionic personality 39 Tuberous Sclerosis 39 hormone imbalances 39 Patau syndrome 39 thyroid hormone deficiency 39 homozygous FH 39 defective gene 39 Degenerative disc disease 39 Anencephaly 39 Major depressive disorder 39 multisystem disease 39 Down syndrome cerebral palsy 39 pseudotumor cerebri 39 schwannoma 39 OCD obsessive compulsive disorder 39 involuntary tics 39 tricuspid atresia 39 born prematurely 39 dystrophies 39 Erb Palsy 39 Krabbe Disease 39 myocarditis 39 Tay Sachs 39 1 antitrypsin deficiency 39 disability 39 motor neuron diseases 39 Chronic constipation 39 Dyspraxia 39 transverse myelitis 39 IgA deficiency 39 Parkinsons disease 39 severe aplastic anemia 39 pulmonary hypertension 39 dysmotility 39 spontaneous remission 39 Diamond Blackfan Anemia 39 IUGR 39 developmentally delayed 39 prenatally diagnosed 39 MODY 39 pes planus 39 dissociative identity disorder 39 neuro developmental 39 cardiac channelopathies 39 pituitary adenoma 39 osteomyelitis 39 diabetes mellitus T2DM 39 HNPCC 39 mastocytosis 39 degenerative neurological condition 39 hallux valgus 39 menopause andropause 39 chordoma 39 developmental trajectories 39 Shy Drager syndrome 39 achalasia