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76 Possible Causes for Cardiomyopathy, Green Jaundice, Poor Feeding

  • 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] […] speech Unsteady gait Increased connective tissue Feeding difficulties Facial hypotonia Achilles tendon contracture Respiratory failure Reduced vital capacity Difficulty standing[mendelian.co]

  • Combined Oxidative Phosphorylation Deficiency Type 3

    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] […] and Arrhythmogenic right ventricular cardiomyopathy, as well as many others.[books.google.com] At 2 months old, she developed paroxysms of irritability that evolved into a persistently irritable state with inconsolable crying, opisthotonic posturing, feeding difficulties[frontiersin.org]

  • 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] Learn more about how to achieve it with Mendelian Learn more Other signs and symptoms that you may find interesting Feeding difficulties and Corneal dystrophy, related diseases[mendelian.co]

  • Neonatal Jaundice

    Paediatrics 27 Jun, 2017 0 Patrick Green Introduction Neonatal Jaundice is very common, with 60% of babies being jaundiced at some point.[almostadoctor.co.uk] […] and patent ductus arteriosus, it causes short-term adverse effects including gastro-intestinal bleeding, intestinal perforation, hyperglycaemia, hypertension, hypertrophic cardiomyopathy[aetna.com] feeding birth trauma e.g. cephalohematoma or instrument delivery prior sibling with jaundice[neonatalhyperbilirubinemia.org]

  • 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] Genetics Home Reference provides information about familial dilated cardiomyopathy.[ghr.nlm.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] 1A Dilated cardiomyopathy 1A Dilated cardiomyopathy 1AA Dilated cardiomyopathy 1BB Dilated cardiomyopathy 1C Dilated cardiomyopathy 1D Dilated cardiomyopathy 1E Dilated cardiomyopathy[pentacorelab.hu] Difficulties, and Delayed Brain Myelination 1 Neurodevelopmental Disorder with Involuntary Movements 1 Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Brain[preventiongenetics.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] difficulties Low-set ears Rare Symptoms - Less than 30% cases Thin upper lip vermilion Retrognathia Spasticity Frontal bossing Delayed skeletal maturation Hydronephrosis[mendelian.co]

  • 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] […] horizontal gaze paresis: 48% Duane retraction syndrome : 34% Congenital fibrosis of extraocular muscles : 9% Bulbar Palate and pharynx dysfunction: 56% Dysarthria, nasal Poor[neuromuscular.wustl.edu] […] anomalies-distal phalangeal hypoplasia Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome Severe intellectual disability-progressive[se-atlas.de]

  • 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] Newborn infants with NS usually have feeding problems resulting in poor growth and delayed bone growth.[centogene.com]

  • 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] Cardiomyopathy hypogonadism collagenoma syndrome 0 *Collagen Diseases *Hypogonadism *Cardiomyopathies *Skin Neoplasms.[reference.md] difficulties, hypothyroidism, hypogonadism, etc.[ojrd.biomedcentral.com]

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