Increased serum ferritin
Symptom Information:
Symptom ID: | HPO:0003281 | |||||||||||||||||||||||
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 metabolism/homeostasis(HPO:0001939) Abnormality of ion homeostasis(HPO:0003111) Abnormality of cation homeostasis(HPO:0010929) Abnormality of transition element cation homeostasis(HPO:0011030) Abnormality of iron homeostasis(HPO:0011031) Increased serum ferritin(HPO:0003281) MedDRA: Investigations(MedDRA:10022891) Water, electrolyte and mineral investigations(MedDRA:10047843) Mineral and electrolyte analyses(MedDRA:10027637) Increased serum ferritin(HPO:0003281) |
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Database Frequency: | 32 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS | (OMIM:616050) |
Aceruloplasminemia | (Orphanet:48818) |
Adult-onset autosomal recessive sideroblastic anemia | (Orphanet:255132) |
Autosomal recessive sideroblastic anemia | (Orphanet:260305) |
Bifunctional enzyme deficiency | (Orphanet:300) |
Congenital atransferrinemia | (Orphanet:1195) |
Dehydrated hereditary stomatocytosis | (Orphanet:3202) |
FTH1-related iron overload | (Orphanet:247790) |
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
GRACILE syndrome | (Orphanet:53693) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4 | (OMIM:603552) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5 | (OMIM:613101) |
HEMOSIDEROSIS, PULMONARY, WITH DEFICIENCY OF GAMMA-A GLOBULIN | (OMIM:235500) |
Hemochromatosis type 2 | (Orphanet:79230) |
Hemochromatosis type 3 | (Orphanet:225123) |
Hemochromatosis type 4 | (Orphanet:139491) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hemochromatosis, type 2B | (OMIM:613313) |
Hemochromatosis, type 5 | (OMIM:615517) |
Hereditary hyperferritinemia with congenital cataracts | (Orphanet:163) |
Lysinuric protein intolerance | (Orphanet:470) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
Neonatal hemochromatosis | (Orphanet:446) |
Rare hereditary hemochromatosis | (Orphanet:220489) |
Severe congenital hypochromic anemia with ringed sideroblasts | (Orphanet:300298) |
X-linked lymphoproliferative disease | (Orphanet:2442) |