Polycythemia
Symptom Information:
Symptom ID: | HPO:0001901 | ||||||||||||||||||||||||||||
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) Polycythemia(HPO:0001901) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Red blood cell disorders(MedDRA:10038158) Polycythemia(HPO:0001901) |
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Database Frequency: | 16 / 7739 | ||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ADENOSINE TRIPHOSPHATE, ELEVATED, OF ERYTHROCYTES | (OMIM:102900) |
Chuvash erythrocytosis | (Orphanet:238557) |
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome | (Orphanet:309854) |
ERYTHROCYTOSIS, FAMILIAL, 3 | (OMIM:609820) |
Fumaric aciduria | (Orphanet:24) |
HEMOGLOBIN--ALPHA LOCUS 1 | (OMIM:141800) |
HEMOGLOBIN--BETA LOCUS | (OMIM:141900) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
Idiopathic pulmonary alveolar proteinosis | (Orphanet:747) |
PERICARDIAL EFFUSION, CHRONIC | (OMIM:260900) |
Primary familial polycythemia | (Orphanet:90042) |
Recessive hereditary methemoglobinemia type 1 | (Orphanet:139373) |
Recessive hereditary methemoglobinemia type 2 | (Orphanet:139380) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER | (OMIM:187300) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
Von Hippel-Lindau disease | (Orphanet:892) |