Hypoproteinemia

Symptom Information:

Symptom ID: HPO:0003075
Synonyms:
Hypoproteinemia (disorder) [Orphanet:49040]
Decreased serum protein level (finding) [Orphanet:49040]
Serum proteins low (finding) [Orphanet:49040]
Hypoproteinemia [Orphanet:49040]
Protein total decreased [Orphanet:49040]
Serum proteins low [Orphanet:49040]
Hypoproteinemia [OMIM:Hypoproteinemia]
Serum protein decreased [Orphanet:49040]
Hypoproteinaemia [Orphanet:49040]
Protein total decreased [MedDRA:10037014]
Proteins serum plasma low [MedDRA:10037014]
Serum protein decreased [MedDRA:10037014]
Serum total protein decreased [MedDRA:10037014]
Total protein low [MedDRA:10037014]
Hypoproteinaemia [MedDRA:10021083]
Hypoproteinemia [MedDRA:10021083]
Decreased total protein [OMIM:Decreased total protein]
Hypoproteinemia (in 1 patient) [OMIM:Hypoproteinemia (in 1 patient)]
Low serum protein [OMIM:Low serum protein]
Quality:
Cross references:
Orphanet:49040 "Hypoproteinemia" [Orphanet:49040]
OMIM: "Hypoproteinemia" [OMIM:Hypoproteinemia]
OMIM: "Decreased total protein" [OMIM:Decreased total protein]
OMIM: "Hypoproteinemia (in 1 patient)" [OMIM:Hypoproteinemia (in 1 patient)]
OMIM: "Low serum protein" [OMIM:Low serum protein]
UMLS:C0020639 "Hypoproteinemia" [HPO:0003075]
UMLS:C0020639 "Hypoproteinemia" [Orphanet:49040]
UMLS:C0860901 "Protein total decreased" [Orphanet:49040]
UMLS:C0392692 "Serum proteins low" [Orphanet:49040]
Is a (Direct Parents):
MedDRA Protein metabolism disorders NEC
HPO         Abnormality of circulating protein level
MedDRA Protein analyses NEC
Orphanet Abnormality of metabolism/homeostasis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of circulating protein level(HPO:0010876)
             Hypoproteinemia(HPO:0003075)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Protein and amino acid metabolism disorders NEC(MedDRA:10037008)
       Protein metabolism disorders NEC(MedDRA:10037009)
          Hypoproteinemia(HPO:0003075)
Investigations(MedDRA:10022891)
    Protein and chemistry analyses NEC(MedDRA:10037000)
       Protein analyses NEC(MedDRA:10036998)
          Hypoproteinemia(HPO:0003075)
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

Aplasia cutis congenita - intestinal lymphangiectasia (Orphanet:1116)
Congenital enteropathy due to enteropeptidase deficiency (Orphanet:168601)
Congenital nephrotic syndrome, Finnish type (Orphanet:839)
Cronkhite-Canada syndrome (Orphanet:2930)
DPAGT1-CDG (Orphanet:86309)
Deafness - small bowel diverticulosis - neuropathy (Orphanet:3217)
Dengue fever (Orphanet:99828)
ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY (OMIM:600351)
ENTEROPATHY, PROTEIN-LOSING (OMIM:226300)
Familial hemophagocytic lymphohistiocytosis (Orphanet:540)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 (OMIM:267700)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 (OMIM:603553)
HYPOPROTEINEMIA, HYPERCATABOLIC (OMIM:241600)
Hemorrhagic fever - renal syndrome (Orphanet:340)
Johanson-Blizzard syndrome (Orphanet:2315)
Menetrier disease (Orphanet:2494)
Mulibrey nanism (Orphanet:2576)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Neonatal hemochromatosis (Orphanet:446)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
Omenn syndrome (Orphanet:39041)
PANCREATIC INSUFFICIENCY, COMBINED EXOCRINE (OMIM:260450)
Pierson syndrome (Orphanet:2670)
Primary intestinal lymphangiectasia (Orphanet:90362)
Proximal myotonic myopathy (Orphanet:606)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
TRYPSINOGEN DEFICIENCY (OMIM:614044)