Prolonged neonatal jaundice

Symptom Information:

Symptom ID: HPO:0006579
Synonyms:
JAUNDICE, NEONATAL [HPO:0006579]
Neonatal jaundice [HPO:0006579]
Jaundice, neonatal [OMIM:Jaundice, neonatal]
Neonatal jaundice [OMIM:Neonatal jaundice]
Prolonged neonatal jaundice [OMIM:Prolonged neonatal jaundice]
Jaundice, neonatal (in some patients) [OMIM:Jaundice, neonatal (in some patients)]
Jaundice neonatal [MedDRA:10023138]
Quality:
Cross references:
OMIM: "Jaundice, neonatal" [OMIM:Jaundice, neonatal]
OMIM: "Neonatal jaundice" [OMIM:Neonatal jaundice]
OMIM: "Prolonged neonatal jaundice" [OMIM:Prolonged neonatal jaundice]
OMIM: "Jaundice, neonatal (in some patients)" [OMIM:Jaundice, neonatal (in some patients)]
Is a (Direct Parents):
HPO         Jaundice
MedDRA Neonatal hepatobiliary disorders
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the liver(HPO:0001392)
                Abnormality of the biliary system(HPO:0004297)
                   Cholestasis(HPO:0001396)
                      Jaundice(HPO:0000952)
                         Prolonged neonatal jaundice(HPO:0006579)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Dermatological manifestations of systemic disorders(HPO:0001005)
                   Jaundice(HPO:0000952)
                      Prolonged neonatal jaundice(HPO:0006579)
MedDRA:
Pregnancy, puerperium and perinatal conditions(MedDRA:10036585)
    Neonatal and perinatal conditions(MedDRA:10028920)
       Neonatal hepatobiliary disorders(MedDRA:10028942)
          Prolonged neonatal jaundice(HPO:0006579)
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

AICARDI-GOUTIERES SYNDROME 1 (OMIM:225750)
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY (OMIM:300908)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Argininemia (Orphanet:90)
Congenital bile acid synthesis defect type 4 (Orphanet:79095)
Congenital dyserythropoietic anemia type I (Orphanet:98869)
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency (Orphanet:93583)
Cytomegalic congenital adrenal hypoplasia (Orphanet:95702)
Galactosemia (Orphanet:352)
Hereditary North American Indian childhood cirrhosis (Orphanet:168583)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
NIEMANN-PICK DISEASE, TYPE C1 (OMIM:257220)
NIEMANN-PICK DISEASE, TYPE C2 (OMIM:607625)
Navajo neurohepatopathy (Orphanet:255229)
Neonatal hemochromatosis (Orphanet:446)
Niemann-Pick disease type A (Orphanet:77292)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
PITUITARY HORMONE DEFICIENCY, COMBINED, 1 (OMIM:613038)
Prolidase deficiency (Orphanet:742)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Thrombotic thrombocytopenic purpura (Orphanet:54057)
Zellweger syndrome (Orphanet:912)