Informaţii despre

Nume Anencephaly
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Anencephaly
Clasificare anatomică Malacards Boli neuronale

Vezi şi

Boli A-Z Acardia Acrocallosal Syndrome Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Amniotic Band Syndrome Anhaptoglobinemia Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ayme-Gripp Syndrome Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Branchiootic Syndrome 1 Brittle Bone Disorder Cephalic Disorders Cerebritis Cerebrovascular Disease Cervical Spina Bifida Aperta Cervical Spina Bifida Cystica Cervicitis Cervicothoracic Spina Bifida Aperta Cervicothoracic Spina Bifida Cystica Chiari Malformation Chromosomal Triplication Chromosome 20p Duplication Chromosome 8p Duplication Cleft Lip Common Cold Cone-Rod Dystrophy 2 Congenital Nervous System Abnormality Craniorachischisis Cystic Lymphangioma Diprosopus Down Syndrome Eclampsia Ectopia Cordis Encephalocele Epidermolysis Bullosa, Junctional, Herlitz Type Exencephaly Fanconi Anemia, Complementation Group E Gastroschisis Hepatic Adenomas, Familial Holoprosencephaly Homocysteinemia Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Hydranencephaly Hydrocephalus Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 Hypercholesterolemia, Autosomal Dominant, 3 Hyperinsulinism Hypoadrenocorticism, Familial Hypospadias Influenza Iniencephaly Klippel-Feil Syndrome Limb Reduction Defect Lumbosacral Spina Bifida Aperta Lumbosacral Spina Bifida Cystica Macular Dystrophy, Retinal, 1, North Carolina Type Megaloblastic Anemia Meningitis Meningocele Methylmalonic Aciduria and Homocystinuria, Cblc Type Methylmalonic Aciduria and Homocystinuria Type Cble Methylmalonic Aciduria and Homocystinuria Type Cblg Methylmalonic Aciduria, Cblb Type Microcephaly Mungan Syndrome Myelomeningocele Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neuronitis Nondisjunction Omphalocele Patau Syndrome Persistent Idiopathic Facial Pain Persistent Vegetative State Polydactyly Polyhydramnios Porencephaly Porphyria Variegata Pre-Eclampsia Prostatitis Psoriasis 2 Psoriasis 7 Ring Chromosome 13 Ring Chromosome 18 Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly Sirenomelia Syringomyelia Teratoma Tetraamelia Syndrome, Autosomal Recessive Thoracolumbosacral Spina Bifida Aperta Thoracolumbosacral Spina Bifida Cystica Thyroiditis Tietz Albinism-Deafness Syndrome Total Spina Bifida Aperta Total Spina Bifida Cystica Toxoplasmoză Transcobalamin Ii Deficiency Trichohepatoenteric Syndrome 1 Upper Thoracic Spina Bifida Aperta Upper Thoracic Spina Bifida Cystica Ventricular Fibrillation, Paroxysmal Familial, 1 Xk Aprosencephaly Yemenite Deaf-Blind Hypopigmentation Syndrome