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64 Possible Causes for Hearing Impairment, Hyperbiliverdinemia

  • 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] […] loss. 0000684 Gingival fibromatosis 0000169 Gingival overgrowth Gum enlargement 0000212 Sensorineural hearing impairment 0000407 Percent of people who have these symptoms[rarediseases.info.nih.gov] […] is not available through HPO Autosomal dominant inheritance 0000006 Progressive sensorineural hearing impairment 0000408 Showing of 6 Last updated: 5/1/2019 The exact, underlying[rarediseases.info.nih.gov]

  • 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] Names and Terminology for IVIC syndrome Other Names : Instituto Venezolano de Investigaciones Cientificas syndrome; Radial ray defects, hearing impairment, external ophthalmoplegia[familydiagnosis.com] Showing of 31 80%-99% of people have these symptoms Hearing impairment Deafness Hearing defect [ more ] 0000365 Hypoplasia of the radius Underdeveloped outer large forearm[rarediseases.info.nih.gov]

  • Pelviscapular 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] Symptoms List: Pelviscapular dysplasia Symptoms and clinical features may include: 1 Clinical Features of Pelviscapular dysplasia : Macrocephaly Hypertelorism Hearing impairment[familydiagnosis.com] impairment Deafness Hearing defect [ more ] 0000365 Hypertelorism Wide-set eyes Widely spaced eyes [ more ] 0000316 Low posterior hairline Low hairline at back of neck 0002162[rarediseases.info.nih.gov]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    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] Stickler syndrome Hearing impairment Treacher Collins-Franceschetti syndrome Hearing impairment Usher syndrome Hearing impairment Waardenburg syndrome Hearing impairment[genomediagnosticsnijmegen.nl] ACRODYSOSTOSIS Is also known as acrodysplasia; arkless-graham syndrome; maroteaux-malamut syndrome Related symptoms: Intellectual disability Short stature Hearing impairment[mendelian.co]

  • Craniodiaphyseal Dysplasia

    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] impairment ; Hypertelorism ; Increased intracranial pressure ; Infantile onset ; Macrocephaly ; Mandibular prognathia ; Optic atrophy ; Papilledema ; Progressive ; Progressive[mousephenotype.org] impairment Abnormality of the ribs Epilepsy Mental retardation Increased intracranial pressure Short stature Macrocephaly Cognitive impairment Sclerosis of the expanded diaphyses[ehealthhall.com]

  • Ehlers-Danlos Syndrome Musculocontractural Type 1

    Maturity onset diabetes of the young, type 11, BLM Bloom syndrome, BLNK Agammaglobulinemia 4, BLOC1S3 Hermansky Pudlak syndrome 8, BLOC1S6 Hermansky pudlak syndrome 9, BLVRA Hyperbiliverdinemia[healthdocbox.com] Strabismus, refractive errors, and elevated intraocular pressure, as well as hearing impairment are common in these patients.[oxfordmedicine.com] […] young, type 11, BLM % 100% Bloom syndrome BLNK % 100% Agammaglobulinemia 4, BLOC1S % 68% Hermansky-Pudlak syndrome 8, BLOC1S % 92% Hermansky-pudlak syndrome 9, BLVRA % 99% Hyperbiliverdinemia[docplayer.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] Abnormality of the cerebral white matter Cerebral calcification Brain atrophy Short stature Hearing impairment Growth delay Cerebral atrophy Delayed speech and language development[mendelian.co] 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]

  • 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] impairment Niemann-Pick disease type A Niemann-Pick disease type C Niemann-Pick disease type C, adult neurologic onset Niemann-Pick disease type C, juvenile neurologic onset[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]

  • Hypomandibular Faciocranial Dysostosis

    Hyperbilirubinemia, Rotor Type; HBLRR OMIM:237800 Hyperbilirubinemia, Shunt, Primary; PSHB OMIM:237900 Hyperbilirubinemia, Transient Familial Neonatal; HBLRTFN OMIM:614156 Hyperbiliverdinemia[informatics.jax.org] impairment Sensorineural hearing impairment Ptosis Flexion contracture Tics Short nose Camptodactyly of finger Blepharophimosis Wide nose Bilateral sensorineural hearing[mendelian.co] Related symptoms: Autosomal recessive inheritance Global developmental delay Short stature Hearing impairment Microcephaly SOURCES: UMLS MONDO OMIM More info about SHORT STATURE[mendelian.co]

  • Generalized Resistance to Thyroid Hormones

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] impairment, and decrease bone mass.[cjhr.org] Clinical features Affected individuals may have delayed growth and puberty, and in severe cases: failure to thrive, mental retardation, infertility, myopathy, hearing impairment[flipper.diff.org]

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