Informaţii despre

Nume Cerebellar Hypoplasia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Other reduction deformities of brain
Clasificare anatomică Malacards Boli neuronale

Vezi şi

Boli A-Z Adie Pupil Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Anterior Horn Cell Disease Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Autism Band Heterotopia Biliary Atresia Blood Group--Ahonen Blood Group, I System Brittle Bone Disorder Capillary Hemangioma Cataract Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 Cerebellar Hypoplasia Tapetoretinal Degeneration Cerebellar Hypoplasia with Endosteal Sclerosis Cerebritis Chiari Malformation Cholera Choroiditis Chromosomal Triplication Chromosome 17p13.3, Centromeric, Duplication Syndrome Cohen Syndrome Colobomatous Microphthalmia Communicating Hydrocephalus Congenital Cytomegalovirus Congenital Hypothyroidism Congenital Lymphedema Congenital Oculomotor Nerve Palsy Congenital Torticollis Cornelia De Lange Syndrome Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia Cri-Du-Chat Syndrome Cytomegalovirus Infection Diabetes Mellitus Diarrhea Down Syndrome Duane Retraction Syndrome 1 Dyskeratosis Congenita Dystonia Ear Malformation Encephalitozoonosis Encephalopathy Epilepsy Epileptic Encephalopathy, Early Infantile, 15 Epileptic Encephalopathy, Early Infantile, 7 Glioma Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Goldberg-Shprintzen Syndrome Headache Hemangioma Hemifacial Microsomia Hepatic Adenomas, Familial Holoprosencephaly Hydranencephaly Hydrocephalus Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypospadias Hypothalamic Hamartomas Hypotonia Ichthyosis Inherited Metabolic Disorder Intrauterine Infections Isolated Complex Iii Deficiency Kid Syndrome Learning Disability Lissencephaly Lissencephaly 1 Lissencephaly 4 Lissencephaly with Cerebellar Hypoplasia Lissencephaly, X-Linked, 1 Lymphedema Lymphocytic Choriomeningitis Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia Microcephaly Microlissencephaly Microphthalmia Microphthalmia, Isolated 2 Moebius Syndrome Mucositis Muscular Atrophy Muscular Dystrophy Myopathy Neonatal Diabetes Mellitus Neuroaxonal Dystrophy Neurofibromatosis, Type Iv, of Riccardi Neuronal Migration Disorders Neuronitis Neuropathy Osteogenesis Imperfecta, Type Iii Oto-Palatal-Digital Syndrome Pachygyria Pancreatic and Cerebellar Agenesis Pancytopenia Periventricular Nodular Heterotopia Phace Syndrome Polydactyly Polymicrogyria Pontocerebellar Hypoplasia, Type 1c Porencephaly Porencephaly, Cerebellar Hypoplasia, and Internal Malformations Prader-Willi Syndrome Ptosis Reflex Epilepsy Renal Hypoplasia Retinal Degeneration Retinitis Retinitis Pigmentosa Ring Chromosome 6 Spinal Muscular Atrophy Spinocerebellar Ataxia 29 Subcortical Band Heterotopia Torticollis Tremor Trigeminal Neuralgia Trisomy 17 Mosaicism Walker-Warburg Syndrome X-Linked Intellectual Disability, Najm Type