Informaţii despre

Nume Septooptic Dysplasia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Bolile canceroase
Clasificari ICD10 Other specified congenital malformations of brain; Septo-optic dysplasia
Clasificare anatomică Malacards Boli ale ochiului; Boli endocrine; Boli neuronale

Vezi şi

Boli A-Z Absence of Septum Pellucidum Adams-Oliver Syndrome Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Angiomyolipoma Aniridia 1 Anorchia Anorexia Nervosa 1 Apert Syndrome Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Autism Autism Spectrum Disorder Autosomal Genetic Disease Blood Group--Ahonen Borjeson-Forssman-Lehmann Syndrome Cerebellar Hypoplasia Cerebral Palsy Cerebritis Cholangiocarcinoma Choroiditis Chromosomal Triplication Clubfoot Combined Pituitary Hormone Deficiencies, Genetic Forms Combined Pituitary Hormone Deficiency Congenital Hepatic Fibrosis Cornelia De Lange Syndrome Cortical Dysplasia, Complex, with Other Brain Malformations 7 Diabetes Insipidus Dilated Cardiomyopathy Dwarfism Dyskinetic Cerebral Palsy Encephalocele Epilepsy Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome Fanconi Anemia, Complementation Group E Frontonasal Dysplasia 1 Gastroschisis Growth Hormone Deficiency Headache Hemophagocytic Lymphohistiocytosis Hepatic Adenomas, Familial Hepatitis Holoprosencephaly Hydranencephaly Hyperinsulinemic Hypoglycemia, Familial, 3 Hyperinsulinemic Hypoglycemia, Familial, 4 Hyperinsulinism Hyperprolactinemia Hypoglycemia Hypopituitarism Hypothyroidism, Congenital, Nongoitrous, 4 Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function Hypotonia Intrahepatic Cholangiocarcinoma Isolated Growth Hormone Deficiency Isolated Growth Hormone Deficiency, Type Iii Kallmann Syndrome Learning Disability Lissencephaly Marshall-Smith Syndrome Neonatal Jaundice Neonatal Thyrotoxicosis Oliver Syndrome Omphalocele Optic Nerve Hypoplasia, Bilateral Pagon Stephan Syndrome Parkinson Disease 15, Autosomal Recessive Early-Onset Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Pituitary Gland Disease Pituitary Hormone Deficiency, Combined, 2 Pituitary Hypoplasia Pituitary Stalk Interruption Syndrome Pituitary Tumors Polymicrogyria Retinal Detachment Retinitis Sarcomatous Intrahepatic Cholangiocarcinoma Schizencephaly Semilobar Holoprosencephaly Septo-Optic Dysplasia Spectrum Sotos Syndrome 1 Three M Syndrome 1 Thyroiditis Valproate Embryopathy Waardenburg Syndrome, Type 1 Yemenite Deaf-Blind Hypopigmentation Syndrome