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31 Possible Causes for Cardiomyopathy, Delayed Speech and Language Development, Green Jaundice

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    […] to 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1-SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] , Dilated, 1ee MYH6 Cardiomyopathy, Dilated, 1g TTN Cardiomyopathy, Dilated, 1y TPM1 Cardiomyopathy, Familial Hypertrophic, 1 MYH6 Cardiomyopathy, Familial Hypertrophic, 14[selfdecode.com] Cerebral atrophy Delayed speech and language development Clonus Gliosis Myoclonus Death in infancy Polyhydramnios Cerebellar hypoplasia Neuronal loss in central nervous system[mendelian.co]

  • 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] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com] Reduced maximal inspiratory pressure Growth delay Delayed speech and language development Carious teeth Intrauterine growth retardation Myopia Renal insufficiency Dystonia[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] 1A Dilated cardiomyopathy 1A Dilated cardiomyopathy 1AA Dilated cardiomyopathy 1BB Dilated cardiomyopathy 1C Dilated cardiomyopathy 1D Dilated cardiomyopathy 1E Dilated cardiomyopathy[pentacorelab.hu] speech and language development Cataract Generalized hirsutism Acanthosis nigricans Hyperinsulinemia Polycystic ovaries Hypospadias Growth hormone excess Round face Ketoacidosis[mendelian.co]

  • 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] Diseases related with Cardiomyopathy and Short phalanx of finger In the following list you will find some of the most common rare diseases related to Cardiomyopathy and Short[mendelian.co] Although she presented language development delay, she exhibited a dysarthria-like speech and mild learning disabilities; however, IQ test results were within the normal range[dovepress.com]

  • Waters-West Syndrome

    21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1- SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] 1A 6 Dilated Cardiomyopathy 1Aa 6 Dilated Cardiomyopathy 1BB 1 Dilated Cardiomyopathy 1C 6 Dilated Cardiomyopathy 1CC 6 Dilated Cardiomyopathy 1D 4 Dilated Cardiomyopathy[preventiongenetics.com] speech and language development Autism Facial asymmetry Abnormality of the kidney Prominent nose Cortical visual impairment Horizontal nystagmus Pineal cyst Ventricular septal[mendelian.co]

  • 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] 1A 6 Dilated Cardiomyopathy 1Aa 6 Dilated Cardiomyopathy 1BB 1 Dilated Cardiomyopathy 1C 6 Dilated Cardiomyopathy 1CC 6 Dilated Cardiomyopathy 1D 4 Dilated Cardiomyopathy[preventiongenetics.com] speech and language development High palate Nystagmus Generalized hypotonia Scarring Seizures Duodenal polyposis Aplastic colon Rectal polyposis Ichthyosis Desmoid tumors[mendelian.co]

  • 2-Aminoadipic 2-Oxoadipic Aciduria

    […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] […] homocystinuria Hydroxykynureninuria Hydroxyprolinemia hyperhomocysteinemia Hyperleucine-Isoleucinemia hyperlysinemia hypermethioninemia Hyperprolinemias Hypertaurinuric Cardiomyopathy[rgd.mcw.edu] speech and language development ; Generalized hypotonia ; Global developmental delay ; Intellectual disability, mild ; Microcephaly ; Phenotypic variability Associated Genes[mousephenotype.org]

  • Hypospadias - Intellectual Disability Syndrome Type Goldblatt

    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] Food and Drug Administration granted Priority Review to Pfizer for its application to market tafamidis, its treatment for transthyretin amyloid cardiomyopathy (ATTR-CM), a[globalgenes.org] speech and language development Autism Facial asymmetry Abnormality of the kidney Prominent nose Cortical visual impairment Horizontal nystagmus Pineal cyst Ventricular septal[mendelian.co]

  • 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] Hypertrophic cardiomyopathy[?] Hypertrophic hemangiectasia[?] Hypertrophic myocardiopathy[?] Hypertrophic osteoarthropathy, primary or idiopathic[?][encyclopedia.kids.net.au] […] skeletal maturation Tracheomalacia Growth delay Microglossia Ventriculomegaly Myopia Proboscis Delayed speech and language development Mandibular aplasia Aglossia Frontal[mendelian.co]

  • 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] speech and language development Downslanted palpebral fissures Long philtrum Abnormality of the dentition Alopecia Brachycephaly Clinodactyly Congenital hip dislocation Short[mendelian.co] […] del Cardiomyopathy, dilated, with premature ovarian failure LMNA del Cardiomyopathy, dilated, with primary testicular failure LMNA del Cardiomyopathy, familial hypertrophic[uniklinik-freiburg.de]

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