Hypoalbuminemia
Symptom Information:
| Symptom ID: | HPO:0003073 | ||||
| Synonyms: |
|
||||
| Quality: | |||||
| Cross references: |
|
||||
| Is a (Direct Parents): |
|
||||
| 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) Abnormal albumin level(HPO:0012116) Hypoalbuminemia(HPO:0003073) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Protein and amino acid metabolism disorders NEC(MedDRA:10037008) Protein metabolism disorders NEC(MedDRA:10037009) Hypoalbuminemia(HPO:0003073) |
||||
| Database Frequency: | 40 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| AL amyloidosis | (Orphanet:85443) |
| ANALBUMINEMIA | (OMIM:616000) |
| Acute interstitial pneumonia | (Orphanet:79126) |
| Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
| Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
| Chylomicron retention disease | (Orphanet:71) |
| Congenital lethal erythroderma | (Orphanet:1954) |
| Congenital nephrotic syndrome, Finnish type | (Orphanet:839) |
| Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
| DIARRHEA 7 | (OMIM:615863) |
| ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY | (OMIM:600351) |
| FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1 | (OMIM:603278) |
| FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6 | (OMIM:614131) |
| Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
| Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation | (Orphanet:93214) |
| Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes | (Orphanet:93216) |
| Galloway-Mowat syndrome | (Orphanet:2065) |
| Gaucher disease type 3 | (Orphanet:77261) |
| Generalized juvenile polyposis/juvenile polyposis coli | (Orphanet:329971) |
| HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
| HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
| HYPOPROTEINEMIA, HYPERCATABOLIC | (OMIM:241600) |
| Hennekam syndrome | (Orphanet:2136) |
| Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
| Juvenile polyposis syndrome | (Orphanet:2929) |
| Kawasaki disease | (Orphanet:2331) |
| Leigh syndrome with nephrotic syndrome | (Orphanet:255249) |
| MPI-CDG | (Orphanet:79319) |
| Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
| NEPHROTIC SYNDROME, TYPE 2 | (OMIM:600995) |
| NEPHROTIC SYNDROME, TYPE 3 | (OMIM:610725) |
| NEPHROTIC SYNDROME, TYPE 8 | (OMIM:615244) |
| NEPHROTIC SYNDROME, TYPE 9 | (OMIM:615573) |
| Neonatal hemochromatosis | (Orphanet:446) |
| PMM2-CDG | (Orphanet:79318) |
| Primary systemic amyloidosis | (Orphanet:314701) |
| Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
| Syndromic diarrhea | (Orphanet:84064) |
| TRICHOHEPATOENTERIC SYNDROME 1 | (OMIM:222470) |
| Wilson disease | (Orphanet:905) |