Imerslund-Grasbeck syndrome type 2
- Synonyms
- Imerslund-Gräsbeck syndrome 2; MEGALOBLASTIC ANEMIA, NORWEGIAN TYPE; Megaloblastic anemia 1, Norwegian type
Summary
Available tests
Clinical tests (12 available)
Molecular Genetics Tests
Genes See tests for all associated and related genes
Also known as: IGS2, PRO1028, amnionless, AMN
Summary: amnion associated transmembrane protein
Clinical features
Help- Abnormality of blood and blood-forming tissues
- Anemia
Anemia
- MedGen UID: 1526
- Concept ID: C0002871
- Finding: Disease or Syndrome
Abnormality of blood and blood-forming tissues
- Megaloblastic anemia
Megaloblastic anemia
- MedGen UID: 1527
- Concept ID: C0002888
- Finding: Disease or Syndrome
Abnormality of blood and blood-forming tissues
- Anemia
- Abnormality of metabolism/homeostasis
- Cobalamin deficiency
Cobalamin deficiency
- MedGen UID: 21880
- Concept ID: C0042847
- Finding: Disease or Syndrome
Abnormality of metabolism/homeostasis
- Cobalamin deficiency
- Abnormality of the digestive system
- Diarrhea
Diarrhea
- MedGen UID: 8360
- Concept ID: C0011991
- Finding: Sign or Symptom
Abnormality of the digestive system
- Diarrhea
- Abnormality of the genitourinary system
- Moderate albuminuria
Moderate albuminuria
- MedGen UID: 896933
- Concept ID: C1654921
- Finding: Finding
Abnormality of the genitourinary system
- Proteinuria
Proteinuria
- MedGen UID: 10976
- Concept ID: C0033687
- Finding: Finding
Abnormality of the genitourinary system
- Recurrent urinary tract infections
Recurrent urinary tract infections
- MedGen UID: 120466
- Concept ID: C0262655
- Finding: Disease or Syndrome
Abnormality of the genitourinary system
- Renal insufficiency
Renal insufficiency
- MedGen UID: 332529
- Concept ID: C1565489
- Finding: Disease or Syndrome
Abnormality of the genitourinary system
- Moderate albuminuria
- Abnormality of the musculoskeletal system
- Lumbar kyphosis
Lumbar kyphosis
- MedGen UID: 336792
- Concept ID: C1844818
- Finding: Finding
Abnormality of the musculoskeletal system
- Lumbar kyphosis
- Growth abnormality
- Growth delay
Growth delay
- MedGen UID: 99124
- Concept ID: C0456070
- Finding: Pathologic Function
Growth abnormality
- Growth delay
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