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24 Possible Causes for Hyperbiliverdinemia, Kernicterus

  • Transient Familial Neonatal Hyperbilirubinemia

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de] , hyperbilirubinemic; encephalopathy , jaundice; kernicterus , kernicterus; jaundice , kernicterus; newborn , Kernicterus of newborn, NOS , Kernicterus of newborn NOS Dutch[fpnotebook.com] Developmental Neuropathology Chapter 25: Kernicterus Kernicterus : (bilirubin encephalopathy) characterized by jaundice, acute neurological dysfunction with specific neuronal[emilytam.com]

  • Hereditary North American Indian Childhood Cirrhosis

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de] الصفحة 342 - Odell GB, Storey GNB, Rosenberg LA: Studies in kernicterus: III.[books.google.com] […] in jaundice, often 1st re- infants, kernicterus cognized w/ 1st 3day of life rare fasting Normal Normal Normal Not needed Liver transplant Phenobarbital 67.[slideshare.net]

  • IgG4-Related Hepatopathy

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de] 壊血病 scorbutus 核黄疸 Kernikterus (独), kernicterus, nuclear jaundice 家族性アミロイドーシス familial amyloidosis 家族性アミロイドポリニューロパチー familial amyloidotic polyneuropathy 家族性LCAT欠損症 familial[jsge.or.jp]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] […] dysplasia-brachydactyly and distinctive speech Angioma serpiginosum, X-linked Intellectual deficit - short stature - hypertelorism Cerebellar ataxia ectodermal dysplasia Kernicterus[checkrare.com] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • Hereditary Hyperphosphatasia

    Hyperandrogenism Due to Cortisone Reductase Deficiency HYP625 Hyperbilirubinemia, Rotor Type HYP236 HBLRR Hyperbilirubinemia, Transient Familial Neonatal HYP766 HBLRTFN Hyperbiliverdinemia[malacards.org] Kearns Sayre Syndrome Kennedy Disease Kenny-Caffey Syndrome Keratitis Ichthyosis Deafness Syndrome Keratoconus Keratomalacia Keratosis Follicularis Keratosis, Seborrheic Kernicterus[arrayit.com]

  • Oculootoradial Syndrome

    […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] […] stem dysgenesis, Basilar artery migraine, Benign paroxysmal positional vertigo, Cerebral palsy, Glomus jugulare tumor, Hydrocephalus, Intracranial space-occupying lesion, Kernicterus[wikidoc.org] jaundice Greenberg dysplasia Greig cephalopolysyndactyly syndrome Greither disease Grisart-Destrée syndrome Griscelli disease type 1 Griscelli disease type 2 Griscelli disease[csbg.cnb.csic.es]

  • Gardner-Diamond Syndrome

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] 1932, when Diamond, along with his mentor Kenneth Blackfan, MD, recognized that several different newborn diseases — including fetal hydrops, severe neonatal jaundice and kernicterus[healio.com] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • Intestinal Pseudo-Obstruction - Patent Ductus Arteriosus - Natal Teeth

    […] hsa04975 hsa04977 ] H01474 Acquired generalized lipodystrophy H01475 Lipodystrophy H01909 Hypoinsulinemic hypoglycemia with hemihypertrophy [PATH: hsa04150 hsa04151 ] H01936 Hyperbiliverdinemia[genome.jp] Unfortunately, the immature brain has an increased susceptibility to the neurotoxic effects of high levels of unconjugated bilirubin, and kernicterus can develop in the preterm[pongpdf.com]

  • Hereditary Hypercarotenemia and Vitamin A Deficiency

    Hyperbilirubinemia, Rotor Type; HBLRR OMIM:237800 Hyperbilirubinemia, Shunt, Primary; PSHB OMIM:237900 Hyperbilirubinemia, Transient Familial Neonatal; HBLRTFN OMIM:614156 Hyperbiliverdinemia[informatics.jax.org] 壊血病 scorbutus 核黄疸 Kernikterus (独), kernicterus, nuclear jaundice 家族性アミロイドーシス familial amyloidosis 家族性アミロイドポリニューロパチー familial amyloidotic polyneuropathy 家族性LCAT欠損症 familial[jsge.or.jp] 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1- SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir]

  • Hypertrichotic Osteochondrodysplasia

    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] Avoid in newborns due to the potential for an increase in free bilirubin, jaundice, and development of kernicterus.[livingnaturally.com]

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