Increased serum ferritin

Symptom Information:

Symptom ID: HPO:0003281
Synonyms:
Elevated serum ferritin [HPO:0003281]
Increased ferritin [HPO:0003281]
Increased serum ferritin level [HPO:0003281]
Hyperferritinemia [Orphanet:49180]
Ferritin increased [Orphanet:49180]
Elevated serum ferritin [OMIM:Elevated serum ferritin]
Increased ferritin [OMIM:Increased ferritin]
Increased serum ferritin [OMIM:Increased serum ferritin]
Increased serum ferritin level [OMIM:Increased serum ferritin level]
Hyperferritinemia/iron overload [Orphanet:49180]
Serum ferritin increased [MedDRA:10040250]
Ferritin high [MedDRA:10040250]
Ferritin increased [MedDRA:10040250]
Increased serum ferritin (in some patients) [OMIM:Increased serum ferritin (in some patients)]
Iron overload [MedDRA:10065973]
Organ iron overload [Orphanet:49180]
Iron overload (disorder) [Orphanet:49180]
Hemosiderosis (disorder) [Orphanet:49180]
Iron Overload [Orphanet:49180]
Hemosiderosis [Orphanet:49180]
Hemosiderosis [OMIM:Hemosiderosis]
Hemosiderosis (13%) [OMIM:Hemosiderosis (13%)]
Iron overload (in some patients) [OMIM:Iron overload (in some patients)]
Quality:
Cross references:
Orphanet:49180 "Hyperferritinemia/iron overload" [Orphanet:49180]
OMIM: "Elevated serum ferritin" [OMIM:Elevated serum ferritin]
OMIM: "Increased ferritin" [OMIM:Increased ferritin]
OMIM: "Increased serum ferritin" [OMIM:Increased serum ferritin]
OMIM: "Increased serum ferritin level" [OMIM:Increased serum ferritin level]
OMIM: "Increased serum ferritin (in some patients)" [OMIM:Increased serum ferritin (in some patients)]
OMIM: "Hemosiderosis" [OMIM:Hemosiderosis]
OMIM: "Hemosiderosis (13%)" [OMIM:Hemosiderosis (13%)]
OMIM: "Iron overload (in some patients)" [OMIM:Iron overload (in some patients)]
UMLS:C0743912 "Ferritin increased" [Orphanet:49180]
UMLS:C0282193 "Iron Overload" [Orphanet:49180]
UMLS:C0019114 "Hemosiderosis" [Orphanet:49180]
Is a (Direct Parents):
HPO         Abnormality of iron homeostasis
Orphanet Abnormality of metabolism/homeostasis
MedDRA Mineral and electrolyte analyses
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)
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)