Hypochromia
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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HPO:
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Database Frequency: | 6 / 7739 | |
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All diseases associated with this symptom:
ANEMIA, SIDEROBLASTIC, PYRIDOXINE-RESPONSIVE, AUTOSOMAL RECESSIVE | (OMIM:206000) |
Adult-onset autosomal recessive sideroblastic anemia | (Orphanet:255132) |
Autosomal recessive sideroblastic anemia | (Orphanet:260305) |
Hereditary orotic aciduria | (Orphanet:30) |
Microcytic anemia with liver iron overload | (Orphanet:83642) |
Severe congenital hypochromic anemia with ringed sideroblasts | (Orphanet:300298) |