Congenital hemolytic anemia

Symptom Information:

Symptom ID: HPO:0004804
Synonyms:
Congenital haemolytic anemia [HPO:0004804]
Neonatal hemolytic anemia [HPO:0004804]
Congenital hemolytic anemia [OMIM:Congenital hemolytic anemia]
Neonatal hemolytic anemia (harderoporphyria) [OMIM:Neonatal hemolytic anemia (harderoporphyria)]
Quality:
Cross references:
OMIM: "Congenital hemolytic anemia" [OMIM:Congenital hemolytic anemia]
OMIM: "Neonatal hemolytic anemia (harderoporphyria)" [OMIM:Neonatal hemolytic anemia (harderoporphyria)]
Is a (Direct Parents):
HPO         Hemolytic anemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of erythrocytes(HPO:0001877)
             Anemia(HPO:0001903)
                Anemia due to reduced life span of red cells(HPO:0011895)
                   Hemolytic anemia(HPO:0001878)
                      Congenital hemolytic anemia(HPO:0004804)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

HEMOLYTIC ANEMIA WITH THERMAL SENSITIVITY OF RED CELLS (OMIM:235370)
Hereditary coproporphyria (Orphanet:79273)