Hypoproteinemia
Symptom Information:
Symptom ID: | HPO:0003075 | |||||||||||||||||||
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 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) |
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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) |