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62 Possible Causes for Hyperbiliverdinemia, Learning Disabilities

  • Neuronal Ceroid Lipofuscinosis

    […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] The less severe phenotype was observed in patient IV-19, a 7 year-old female with visual loss since she was six years-old and mild learning disability.[scielo.br] Mild neurologic symptoms then appear, often manifesting as learning disabilities, hypotonia, and hyporeflexia.[ncbi.nlm.nih.gov]

  • Hereditary Hyperekplexia

    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] The majority of individuals with the condition have normal intelligence, but those most severely affected may have a learning disability.[geneticdisordersuk.org] He has learning disabilities for which he is in a special class.[jmg.bmj.com]

  • Familial Recurrent Peripheral Facial Palsy

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] […] syndrome X-linked dystonia-parkinsonism X-linked epilepsy-learning disabilities-behavior disorders syndrome X-linked hereditary sensory and autonomic neuropathy with deafness[se-atlas.de] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • 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] disabilities, autism Gingival enlargement associated with vascular disorders Sturge-Weber syndrome[ 32 ] Unilateral cutaneous nevi, unilateral vascular hyperplasia, neurological[wjgnet.com] disabilities, behavioural disorders and dementia (MPS-III or Sanfilippo syndrome); or (3) as severe bone dysplasia (MPS-4 or Morquio syndrome).[elsevier.es]

  • 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] Most patients have a mild speech delay, and a small percentage have learning difficulties or intellectual disability (summary by {12:van Bon et al., 2012}).[diseaseinfosearch.org] Most patients have a mild speech delay, and a small percentage have learning difficulties or intellectual disability.[uniprot.org]

  • Hypohidrotic Ectodermal Dysplasia

    […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] Disability, and Syndactyly; Rosselli-Gulienetti Syndrome) p. 37 Ellis-van Creveld Syndrome (EVC) p. 39 Weyers Acrofacial Dysostosis Syndrome (Curry-Hall Syndrome) p. 41 Van[booktopia.com.au] Disability, and Syndactyly; Rosselli-Gulienetti Syndrome) 37 (2) 2.3.6 Ellis-van Creveld Syndrome (EVC) 39 (2) 2.3.7 Weyers Acrofacial Dysostosis Syndrome (Curry-Hall Syndrome[kriso.ee]

  • Waters-West Syndrome

    21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1- SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] In addition, some patients have learning disabilities, behavioral problems, psychiatric disorders and hyperactivity.[primaryimmune.org] Mildly affected individuals may only have subtle learning disabilities and physical abnormalities whereas severely affected individuals may have many of the features listed[rarediseasesnetwork.org]

  • Limb-Girdle Muscular Dystrophy Type 1H

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] , severe Hypertonia Abnormality of the skeletal system Kyphosis Cerebellar hypoplasia Recurrent infections Severe short stature Gait ataxia Pes planus Specific learning disability[mendelian.co] Disabilities And Behavior Disorders 3 Epileptic encephalopathy, childhood-onset 6 Epileptic encephalopathy, early infantile, 1 6 Epileptic Encephalopathy, Early Infantile[preventiongenetics.com]

  • Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] disabilities: Some patients ?[neuromuscular.wustl.edu] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • Autosomal Recessive Primary Microcephaly Type 10

    […] to 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1-SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] […] syndrome X-linked epilepsy-learning disabilities-behavior disorders syndrome X-linked hypophosphatemia X-linked intellectual disability due to GRIA3 mutations X-linked intellectual[se-atlas.de] 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]

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