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44 Possible Causes for Brain Death, Hyperbiliverdinemia

  • Neuronal Ceroid Lipofuscinosis

    death.[en.wikipedia.org] […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] , and to prevent the death of some neurons (a type of cell) in the brain.[clinicaltrials.gov]

  • Transient Familial Neonatal Hyperbilirubinemia

    The high levels are poisonous to the brain and can cause death.[nicklauschildrens.org] Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de] Death or severe brain and nervous system (neurological) problems can occur if the condition is not treated. This problem is most often found immediately after delivery.[medlineplus.gov]

  • Limb-Girdle Muscular Dystrophy Type 1H

    104 HypoxicIschemic Encephalopathy in Infants and Older Children E-1849 105 Disorders of Intracranial Pressure E-1868 106 Spinal Cord Injury E-1882 107 Determination of Brain[books.google.com] jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] Death in Infants and Children E-1910 108 Development and Function of the Cerebrovascular System E-1931 109 Arterial Ischemic Stroke in Infants and Children E-1941 110 Sinovenous[books.google.com]

  • Hereditary Hyperekplexia

    The stiffness and startle episodes pose a threat to life as they can lead to injuries, hypoxic episodes, brain injury, and sudden infant death syndrome due to laryngospasm[neurologyindia.com] Joubert syndrome 17 Cardiac conduction defect, nonspecific Lethal multiple pterygium syndrome Non-small cell lung cancer Acroerythrokeratoderma Renal hypodysplasia/aplasia 2 Hyperbiliverdinemia[amp.pharm.mssm.edu] Brain Dev. 1995 ; 17 ( 2 ): 114 –6. 5 Cioni, G, Biagioni, E, Bottai, P, Castellacci, AM, Paolicelli, PB.[cambridge.org]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    […] infarction *cerebral infarction 【脳梗塞後遺症】*sequelae of cerebral infarction[pl] 【脳挫傷】*brain contusion *cerebral contusion 【脳死】*brain death *cerebral death 【脳室炎】*ventriculitis[medo.jp] jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] […] brain stem syndrome 【脳幹損傷】*brain stem injury 【脳血管発作】*cerebrovascular accident (略 CVA) 【脳結石症】*encephalolithiaisis 【脳血栓症】*cerebral thrombosis 【脳硬化症】*cerebrosclerosis 【脳梗塞】*brain[medo.jp]

  • Hypomandibular Faciocranial Dysostosis

    104 HypoxicIschemic Encephalopathy in Infants and Older Children E-1849 105 Disorders of Intracranial Pressure E-1868 106 Spinal Cord Injury E-1882 107 Determination of Brain[books.google.ro] Hyperbilirubinemia, Rotor Type; HBLRR OMIM:237800 Hyperbilirubinemia, Shunt, Primary; PSHB OMIM:237900 Hyperbilirubinemia, Transient Familial Neonatal; HBLRTFN OMIM:614156 Hyperbiliverdinemia[informatics.jax.org] The condition results in severe brain malformations and infant death with...read more » Cornelia de Lange syndrome 1 A very rare disorder involving delayed physical development[wikidoc.org]

  • Autosomal Recessive Primary Microcephaly Type 10

    Brain weight is markedly reduced and the cerebral cortex is disproportionately small.[genecards.org] […] to 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1-SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] Hyperbiliverdinemia, 614156 (3) BLVRB G:600941 . . BLZF1 G:608692 . . BMF G:606266 . . BMI1 G:164831 . . BMIQ1 P:606641 . . BMIQ2 P:606643 . . BMIQ3 P:607446 . .[usegalaxy.org]

  • Waters-West Syndrome

    […] of liver cells or tissue), [14] [18] encephalopathy (brain dysfunction), [18] seizure, [23] and coma. [24] Failure of neurologic, cardiac, renal, and gastrointestinal (GI[en.wikipedia.org] 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1- SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] The most common cause of death is status epilepticus and bronchopneumonia.[atlases.muni.cz]

  • Hypertrichotic Osteochondrodysplasia

    […] infarction *cerebral infarction 【脳梗塞後遺症】*sequelae of cerebral infarction[pl] 【脳挫傷】*brain contusion *cerebral contusion 【脳死】*brain death *cerebral death 【脳室炎】*ventriculitis[medo.jp] Cases 401948 Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency 4 Cases 168588 Hyperandrogenism due to cortisone reductase deficiency 11 Cases 276405 Hyperbiliverdinemia[azkurs.org] […] brain stem syndrome 【脳幹損傷】*brain stem injury 【脳血管発作】*cerebrovascular accident (略 CVA) 【脳結石症】*encephalolithiaisis 【脳血栓症】*cerebral thrombosis 【脳硬化症】*cerebrosclerosis 【脳梗塞】*brain[medo.jp]

  • Hypergonadotropic Hypogonadism-Cataract Syndrome

    [MIM: 606159 ] Hereditary hyperferritinemia-cataract syndrome (HHCS) [MIM: 600886 ] FTO Q9C0B1 non-pleiotropic Growth retardation developmental delay coarse facies early death[sbg.bio.ic.ac.uk] Hyperbilirubinemia, Rotor Type; HBLRR OMIM:237800 Hyperbilirubinemia, Shunt, Primary; PSHB OMIM:237900 Hyperbilirubinemia, Transient Familial Neonatal; HBLRTFN OMIM:614156 Hyperbiliverdinemia[informatics.jax.org] […] dysgenesis 1 (ODG1) [MIM: 233300 ] FTCD O95954 non-pleiotropic Glutamate formiminotransferase deficiency (FIGLU-URIA) [MIM: 229100 ] FTL P02792 pleiotropic Neurodegeneration with brain[sbg.bio.ic.ac.uk]

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