Informaţii despre

Nume Encephalocele
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Encephalocele, unspecified
Clasificare anatomică Malacards Boli neuronale
Boli din aceeaşi familie Basal Encephalocele; Frontal Encephalocele

Vezi şi

Boli A-Z Achondrogenesis Achondrogenesis, Type Ia Adenoma Aging Aicardi Syndrome Al-Gazali-Bakalinova Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Anencephaly Aniridia 1 Anorexia Nervosa 1 Apert Syndrome Arachnoid Cysts Arachnoiditis Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Bacterial Meningitis Baraitser-Winter Syndrome 1 Bardet-Biedl Syndrome Bardet-Biedl Syndrome 13 Bardet-Biedl Syndrome 14 Bardet-Biedl Syndrome 15 Basal Encephalocele Beckwith-Wiedemann Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen 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 Brachial Amelia, Cleft Lip, and Holoprosencephaly Brittle Bone Disorder Cavernous Sinus Thrombosis Cellulitis Cerebritis Cerebrospinal Fluid Leak Cervicitis Chiari Malformation Chiari Malformation Type I Choanal Atresia, Posterior Cholesteatoma Choroiditis Chromosomal Triplication Ciliopathy Cleft Lip Cleft Lip/palate Coach Syndrome Cold-Induced Sweating Syndrome Colonic Atresia Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hepatic Fibrosis Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia Corpus Callosum Lipoma Craniofacial Microsomia Craniosynostosis Crest Syndrome Cri-Du-Chat Syndrome Cryptophthalmos Cystic Teratoma Dandy-Walker Complex Dandy-Walker Syndrome Dermoid Cyst Dk Phocomelia Syndrome Duane Retraction Syndrome 1 Duodenitis Dwarfism Ehlers-Danlos Syndrome Epidermoid Cysts Epilepsy Exencephaly Exophthalmos Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome Fanconi Anemia, Complementation Group E Focal Epilepsy Fraser Syndrome 1 Frontal Encephalocele Frontonasal Dysplasia 1 Glioma Growth Hormone Deficiency Headache Head Injury Hemangioma Hemangioma-Thrombocytopenia Syndrome Hepatitis Holoprosencephaly Hydrocephalus Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydrolethalus Syndrome 1 Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertelorism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypopituitarism Idiopathic Hypertrophic Pachymeningitis Igg4-Related Pachymeningitis Incontinentia Pigmenti Iniencephaly Intestinal Atresia Intracranial Hypertension Isolated Oxycephaly Joubert Syndrome 1 Joubert Syndrome with Oculorenal Anomalies Klippel-Feil Syndrome Knobloch Syndrome Knobloch Syndrome 1 Laryngeal Atresia, Encephalocele, and Limb Deformities Laryngitis Lipomyelomeningocele Locked-in Syndrome Lymphoma Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Malignant Hypertension Malignant Spiradenoma Mast Cell Activation Syndrome Mastoiditis Mature Teratoma Meckel Syndrome, Type 1 Mediastinitis Megalencephaly Meningitis Meningocele Microcephaly Microphthalmia Microphthalmia, Isolated 2 Morning Glory Syndrome Mosaic Trisomy 14 Murcs Association Myelomeningocele Nasal Encephalocele Nasopharyngitis Nephronophthisis Nephronophthisis 3 Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurofibromatosis, Type I Neurofibromatosis, Type Iv, of Riccardi Neuronitis Occipital Encephalocele Omphalocele Opitz Gbbb Syndrome, Type I Opitz Gbbb Syndrome, Type Ii Orbital Cyst Orofaciodigital Syndrome Orofaciodigital Syndrome I Orofaciodigital Syndrome Vi Osteopetrosis Otitis Media Parietal Encephalocele Parietal Foramina Parkinson Disease 15, Autosomal Recessive Early-Onset Penis Agenesis Peritonitis Periventricular Nodular Heterotopia Peters-Plus Syndrome Phocomelia Pilocytic Astrocytoma Pituitary Adenoma Pituitary Hormone Deficiency, Combined, 2 Pneumococcal Meningitis Polycystic Kidney Disease Polycystic Kidney Disease 5 Polydactyly Polymicrogyria Porencephaly Primary Intralymphatic Angioendothelioma Quadriplegia Retinitis Retinochoroidal Coloboma Rubella Schizencephaly Seizure Disorder Semilobar Holoprosencephaly Senior-Løken Syndrome Senior-Loken Syndrome 1 Short-Rib Thoracic Dysplasia 6 with or Without Polydactyly Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Situs Inversus Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Spastic Quadriplegia Spinocerebellar Ataxia 29 Spondyloocular Syndrome Subdural Empyema Subependymal Nodular Heterotopia Superior Semicircular Canal Dehiscence Temporal Lobe Epilepsy Teratoma Tetralogy of Fallot Thanatophoric Dysplasia, Type Ii Three M Syndrome 1 Thrombocytopenia Thrombosis Tuberous Sclerosis Wegener Granulomatosis