Abnormal hemoglobin

Symptom Information:

Symptom ID: HPO:0011902
Synonyms:
Hemoglobinopathy [Orphanet:48340]
Hemoglobinopathy (disorder) [Orphanet:48340]
Hemoglobinopathies [Orphanet:48340]
Hemoglobinosis/hemoglobinopathy [Orphanet:48340]
Haemoglobinopathy [Orphanet:48340]
Haemoglobinopathy [MedDRA:10060892]
Haemoglobinopathy NOS [MedDRA:10060892]
Other haemoglobinopathies [MedDRA:10060892]
Other hemoglobinopathies [MedDRA:10060892]
Hemoglobinopathy [MedDRA:10060892]
Haemoglobinopathies [MedDRA:10018902]
Quality:
Cross references:
Orphanet:48340 "Hemoglobinosis/hemoglobinopathy" [Orphanet:48340]
UMLS:C0019045 "Hemoglobinopathies" [Orphanet:48340]
Is a (Direct Parents):
MedDRA Blood and lymphatic system disorders
HPO         Increased HbA2 hemoglobin
MedDRA Haemoglobinopathies NEC
HPO         Abnormality of erythrocytes
HPO         HbS hemoglobin
Orphanet Abnormality of erythrocytes
HPO         Elevated hemoglobin A1c
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)
             Abnormal hemoglobin(HPO:0011902)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Abnormal hemoglobin(HPO:0011902)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Alpha-thalassemia (Orphanet:846)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Beta-thalassemia (Orphanet:848)
Beta-thalassemia - X-linked thrombocytopenia (Orphanet:231393)
Beta-thalassemia associated with another hemoglobin anomaly (Orphanet:231230)
Beta-thalassemia intermedia (Orphanet:231222)
Beta-thalassemia major (Orphanet:231214)
Congenital amegakaryocytic thrombocytopenia (Orphanet:3319)
Delta-beta-thalassemia (Orphanet:231237)
Dominant beta-thalassemia (Orphanet:231226)
HEMOGLOBIN--ZETA LOCUS (OMIM:142310)
Hb Bart's hydrops fetalis (Orphanet:163596)
Hemoglobin C - beta-thalassemia (Orphanet:231242)
Hemoglobin E - beta-thalassemia (Orphanet:231249)
Hereditary persistence of fetal hemoglobin - beta-thalassemia (Orphanet:46532)
Pearson syndrome (Orphanet:699)
Primary familial polycythemia (Orphanet:90042)