Anemia, mild
Symptom Information:
Symptom ID: | OMIM : No Id available | |||
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Database Frequency: | 6 / 7739 | |||
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All diseases associated with this symptom:
Aceruloplasminemia | (Orphanet:48818) |
Familial benign copper deficiency | (Orphanet:1551) |
HYPERBILIRUBINEMIA, SHUNT, PRIMARY | (OMIM:237800) |
Hyperlysinemia, type I | (OMIM:238700) |
Hyperuricemia - anemia - renal failure | (Orphanet:217330) |
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY | (OMIM:601347) |