Acanthocytosis

Symptom Information:

Symptom ID: HPO:0001927
Synonyms:
Acanthocytes [HPO:0001927]
Red cell acanthocytosis [HPO:0001927]
Acanthocytes [OMIM:Acanthocytes]
Acanthocytosis [OMIM:Acanthocytosis]
Red cell acanthocytosis [OMIM:Red cell acanthocytosis]
Quality:
Cross references:
OMIM: "Acanthocytes" [OMIM:Acanthocytes]
OMIM: "Acanthocytosis" [OMIM:Acanthocytosis]
OMIM: "Red cell acanthocytosis" [OMIM:Red cell acanthocytosis]
UMLS:C0000886 "Acanthocytes" [HPO:0001927]
Is a (Direct Parents):
HPO         Poikilocytosis
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)
             Poikilocytosis(HPO:0004447)
                Acanthocytosis(HPO:0001927)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Abetalipoproteinemia (Orphanet:14)
Choreoacanthocytosis (Orphanet:2388)
HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1 (OMIM:615558)
HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION (OMIM:607236)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5 (OMIM:604777)
Lathosterolosis (Orphanet:46059)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1 (OMIM:109270)
Thrombocytopenia with congenital dyserythropoietic anemia (Orphanet:67044)
WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS (OMIM:278100)