Abnormality of erythrocytes
Symptom Information:
Symptom ID: | HPO:0001877 | ||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | |||||||||||||||||||
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) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Red blood cell disorders(MedDRA:10038158) Red blood cell abnormal findings NEC(MedDRA:10038144) Abnormality of erythrocytes(HPO:0001877) |
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Database Frequency: | 18 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Albers-Schönberg osteopetrosis | (Orphanet:53) |
Autoimmune hemolytic anemia | (Orphanet:98375) |
Autoimmune hemolytic anemia, cold type | (Orphanet:228312) |
Autoimmune hemolytic anemia, warm type | (Orphanet:90033) |
Drug-induced autoimmune hemolytic anemia | (Orphanet:90037) |
Dyschromatosis universalis hereditaria 1 | (OMIM:127500) |
Dyschromatosis universalis hereditaria 2 | (OMIM:612715) |
Dyschromatosis universalis hereditaris 3 | (OMIM:615402) |
Good syndrome | (Orphanet:169105) |
Greenberg dysplasia | (Orphanet:1426) |
Hereditary methemoglobinemia | (Orphanet:621) |
Leukocyte adhesion deficiency | (Orphanet:2968) |
Mixed-type autoimmune hemolytic anemia | (Orphanet:90036) |
Multiple sclerosis - ichthyosis - factor VIII deficiency | (Orphanet:3151) |
Primary familial polycythemia | (Orphanet:90042) |
Secondary polycythemia | (Orphanet:98428) |
TN POLYAGGLUTINATION SYNDROME | (OMIM:300622) |
X-linked sideroblastic anemia | (Orphanet:75563) |