Apert syndrome

Related by string. Apert Syndrome * : Apert / syndromes . Syndromes . SYNDROME . Syndrome : Severe Acute Respiratory Syndrome . Acquired Immune Deficiency Syndrome . Acquired Immune Deficiency Syndromes . chronic fatigue syndrome . irritable bowel syndrome IBS . Irritable Bowel Syndrome IBS . Shy Drager syndrome . Restless Legs Syndrome RLS . Fetal Alcohol Syndrome * *

Related by context. Frequent words. (Click for all words.) 66 polycystic ovary syndrome 65 Klinefelter syndrome 65 congenital disorder 65 DiGeorge syndrome 65 hypoplasia 64 congenital disorders 64 chromosomal disorder 64 Angelman syndrome 63 Spina bifida 63 Retinoblastoma 63 neural tube defect 63 thrombophilia 62 congenital abnormality 62 achondroplasia 62 congenital anomalies 62 developmental abnormalities 62 polycystic ovaries 61 polycystic ovary syndrome PCOS 61 unexplained infertility 61 genetic abnormality 61 ambiguous genitalia 60 congenital abnormalities 60 craniosynostosis 60 dystrophy 60 malformation 59 TTTS 59 osteogenesis imperfecta 59 Leber congenital amaurosis 59 toxemia 59 precocious puberty 59 cryptorchidism 59 Fanconi anemia 59 varicocele 59 bone deformities 59 Hyperthyroidism 58 teratoma 58 genetically inherited 58 sirenomelia 58 congenital malformation 58 thyroid dysfunction 58 atrial septal defect 58 degenerative disorder 58 gastroschisis 58 nephritis 58 muscle degeneration 58 fatal neurodegenerative 58 NF1 58 biliary atresia 57 hirsutism 57 epidermolysis bullosa 57 trisomy 57 Gestational diabetes 57 chromosomal abnormality 57 Muscular dystrophy 57 fetu 57 polycystic ovarian syndrome 57 chromosomal abnormalities 57 autosomal dominant 57 placental abruption 57 Tetralogy 57 Retinopathy 57 beta thalassemia 57 neurological dysfunction 57 Uterine fibroids 57 premature ovarian 57 ependymoma 56 genetic disorder 56 Oxidative stress 56 anencephaly 56 malformations 56 Wilms tumor 56 CFTR gene 56 Marfan syndrome 56 Chronic fatigue 56 Tay Sachs disease 56 hypothyroid 56 hemochromatosis 56 genetic defect 56 neurofibromatosis 56 myotonic dystrophy 56 Pulmonary hypertension 56 recessive genes 56 Marfan Syndrome 56 severely deformed 56 neurodevelopmental disorder 56 estrogen deficiency 56 microcephaly 56 congenital defects 56 BRCA1 mutations 56 dermatomyositis 56 Prader Willi syndrome 56 recessive gene 56 RPE# 56 NF2 56 HNPCC 56 tuberous sclerosis 56 Testicular 56 premature menopause 56 Angelman Syndrome 56 medulloblastomas 55 Congenital heart

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