Acanthocytosis
Symptom Information:
Symptom ID: | HPO:0001927 | |||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |