genetic defect, genetic mutation, genetic disorder, gene mutation, mutation, mutant gene, chromosomal anomaly, abnormalities, myotonic dystrophy, autosomal dominant disorder, congenital anomaly, polydactylism, hydrops, mosaicism, malformation, recessive gene, osteogenesis imperfecta, congenital disorder, histiocytosis, trisomy, autosomal recessive disease, anencephaly, herpesviruses, immunodeficiency, pyloric stenosis, neurofibromas, galactosemia, metabolic disorder, achromatopsia, teratoma, dysgenesis, polydactyly, degenerative disorder, heritable, congenital abnormality, osteopetrosis, severe combined immunodeficiency, monogenic, familial hypercholesterolemia, proband, diaphragmatic hernia, achondroplasia, homozygosity, rh positive, birth defect, toxoplasmosis, aneuploidy, hemochromatosis, monozygotic twin, heterotaxy, idiopathic, myelomeningocele, molar pregnancy, medulloblastoma, roseola, neurological disorder, choriocarcinoma, hyperemesis, blastomeres, angiosarcoma, heterozygous, hyperemesis gravidarum, penetrance, hamartoma, prosopagnosia, cerebri, blastoma, leukodystrophy, hypoplasia, ectopic, hyperinsulinism, nonhereditary, rh incompatibility, xeroderma pigmentosum, herpes simplex encephalitis, retrovirus, otosclerosis, alveolar rhabdomyosarcoma, neuroblastoma, rh factor, thyroiditis, cardiomyopathy, karyotype, gene, embryonal rhabdomyosarcoma, lymphoblastic leukemia, epididymitis, homozygous, phenylketonuria, hyperparathyroidism, rhabdomyosarcoma, klinefelter syndrome, neurofibromatosis, hyperplastic, phenotype, herpes zoster virus, chromosome, ectoderm, lichen planus, orchitis, atresia, lactase deficiency

abetalipoproteinemia, achondroplasia, albers-schonberg disease, autosomal dominant disease, autosomal recessive disease, chondrodystrophy, cystic fibrosis, dwarfism, fallot's tetralogy, fibrocystic disease of the pancreas, gaucher's disease, hypobetalipoproteinemia, juvenile amaurotic idiocy, maple syrup urine disease, marble bones disease, mcardle's disease, mucovioscidosis, muscular dystrophy, nanism, osteopetrosis, pancreatic fibrosis, porphyria, spielmeyer-vogt disease, tetralogy of fallot

disease

congenital disease, genetic disease, genetic disorder, inherited disease, inherited disorder