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23 Possible Causes for Hyperbiliverdinemia, Hyporeflexia

  • 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] […] weakness Trophic changes related to pain Autophagic vacuoles Centrally nucleated skeletal muscle fibers Pica Peripheral neuropathy Distal muscle weakness Flexion contracture Hyporeflexia[mendelian.co] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • Muscular Dystrophy-Dystroglycanopathy Type C12

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] The older sister, aged 25 years, had proximal weakness, calf pseudohypertrophy, hyporeflexia, mild facial weakness, and Gowers sign.[findzebra.com] Joint stiffness Obesity Neonatal hypotonia Pectus excavatum Facial palsy Proximal muscle weakness in lower limbs Feeding difficulties Proximal lower limb amyotrophy Pain Hyporeflexia[mendelian.co]

  • 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] Mild neurologic symptoms then appear, often manifesting as learning disabilities, hypotonia, and hyporeflexia.[ncbi.nlm.nih.gov] 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]

  • 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] .  The diagnosis is suggested by the association of profound hypotonia from muscle weakness, (floppy infant syndrome), hyporeflexia and an enlarged tongue.  The heart is[slideshare.net] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • 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] […] hallux Abnormal heart valve morphology Thin ribs Elevated alkaline phosphatase Bicuspid aortic valve Low anterior hairline Lymphedema Platyspondyly Anxiety Cerebral atrophy Hyporeflexia[mendelian.co]

  • Hypergonadotropic Hypogonadism-Cataract Syndrome

    Hyperbilirubinemia, Rotor Type; HBLRR OMIM:237800 Hyperbilirubinemia, Shunt, Primary; PSHB OMIM:237900 Hyperbilirubinemia, Transient Familial Neonatal; HBLRTFN OMIM:614156 Hyperbiliverdinemia[informatics.jax.org] In the infantile multisystem type, infants show axial hypotonia, hyporeflexia, esotropia, and developmental delay.[ncbi.nlm.nih.gov]

  • 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] Hypoprothrombinemia (congenital) (hereditary) (idiopathic)- K11.7 Hypoptyalism Hypopyon (eye) (anterior chamber) -see Iridocyclitis, acute, hypopyon R68.0 Hypopyrexia R29.2 Hyporeflexia[coding-pro.com] 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1- SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir]

  • 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] […] of the femoral head Pes cavus Pigmentary retinopathy Bradykinesia Increased serum insulin-like growth factor 1 Convex nasal ridge Polyneuropathy Falls Sensory neuropathy Hyporeflexia[mendelian.co]

  • 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] Muscle weakness and hyporeflexia or areflexia may be evident. Histologically and anatomically, the involved muscle demonstrates marked variation in fiber size.[radiologykey.com]

  • 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] Rare Symptoms - Less than 30% cases Muscular hypotonia Anteverted nares Wide nasal bridge Midface retrusion Small for gestational age Birth length less than 3rd percentile Hyporeflexia[mendelian.co] 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]

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