Hypochromia

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Hypochromia" [OMIM:Hypochromia]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 6 / 7739
Resource:

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)