Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandCyanosis (D003490)
Parent Node:
expandLiver Diseases (D008107)
..Starting node
..expandCyanosis and Hepatic Disease (C565660)

       Child Nodes:



 Sister Nodes: 
..expandalpha 1-Antitrypsin Deficiency (D019896) Child1
..expandBudd-Chiari Syndrome (D006502) Child1
..expandCarnitine Palmitoyltransferase II Deficiency, Infantile (C563462)
..expandCholestasis, Intrahepatic (D002780) Child14
..expandCOACH syndrome (C536430)
..expandCongenital Hepatic Fibrosis (C580013)
..expandCyanosis and Hepatic Disease (C565660)
..expandDrug-Induced Liver Injury (D056486) Child2
..expandFatty Liver (D005234) Child6
..expandFocal Nodular Hyperplasia (D020518)
..expandGlycogen Storage Disease 0, Liver (C565485)
..expandGSD IV, Nonprogressive Hepatic (C565540)
..expandHepatic Insufficiency (D048550) Child9
..expandHepatic Veno-Occlusive Disease (D006504) Child1
..expandHepatitis (D006505) Child17
..expandHepatolenticular Degeneration (D006527) Child2
..expandHepatomegaly (D006529) Child4
..expandHepatopulmonary Syndrome (D020065)
..expandHepatorenal Syndrome (D006530)
..expandHypertension, Portal (D006975) Child3
..expandLiver Abscess (D008100) Child2
..expandLiver Cirrhosis (D008103) Child16
..expandLiver Diseases, Alcoholic (D008108) Child3
..expandLiver Diseases, Parasitic (D008109) Child5
..expandLiver Fibrocystic Disease and Polydactyly (C565272)
..expandLiver Neoplasms (D008113) Child8
..expandNavajo neurohepatopathy (C538344) Child1
..expandPeliosis Hepatis (D010382)
..expandPhosphoenolpyruvate carboxykinase deficiency (C536654)
..expandPolycystic liver disease (C536330)
..expandPorphyrias, Hepatic (D017094) Child14
..expandRENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
..expandRetinohepatoendocrinologic Syndrome (C564839)
..expandTuberculosis, Hepatic (D014386)
..expandZellweger Syndrome (D015211) Child3
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:2913
Name:Cyanosis and Hepatic Disease
Definition:
Alternative IDs:
ParentIDs:MESH:D003490|MESH:D008107
TreeNumbers:C06.552/C565660 |C23.888.248/C565660
Synonyms:
Slim Mappings:Digestive system disease|Signs and symptoms
Reference: MedGen: C565660
MeSH: C565660
OMIM: 219400;

Genes:
Phenotypes
1 HP:0000007Autosomal recessive inheritance
2 HP:0001438Abnormal abdomen morphology
3 HP:0001217Clubbing
4 HP:0000961Cyanosis
5 HP:0002094Dyspnea
6 HP:0012115Hepatitis
Disease Causing ClinVar Variants