Hemosiderosis, pulmonary, with deficiency of gamma-a globulin

Preferred Label : Hemosiderosis, pulmonary, with deficiency of gamma-a globulin;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 235500;

Details

Origin ID

235500;

UMLS CUI

C0020807;

Automatic exact mappings (from CISMeF team)
- idiopathic pulmonary hemosiderosis [MeSH Supplementary Concept]
DO Cross reference
- pulmonary hemosiderosis [DO Concept]
HPO term(s)
- Abnormality of the respiratory system [HPO term]
- Autosomal recessive inheritance [HPO term]
- Decreased circulating IgA level [HPO term]
ORDO concept(s)
- Idiopathic pulmonary hemosiderosis [ORDO Disease]
See also inter- (CISMeF)
- Primary Pulmonary Hemosiderosis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Idiopathic pulmonary haemosiderosis [MedDRA LLT]
- Idiopathic pulmonary hemosiderosis [ICD-9 code]
- Idiopathic pulmonary hemosiderosis [ORDO Disease]
- Idiopathic pulmonary hemosiderosis [MedDRA LLT]
- Idiopathic pulmonary hemosiderosis (disorder) [SNOMED CT concept]
- Primary Pulmonary Hemosiderosis [MeSH concept]
- Pulmonary haemosiderosis [MedDRA Preferred Term]
- Pulmonary hemosiderosis [MedDRA LLT]
- idiopathic pulmonary hemosiderosis [MeSH Supplementary Concept]
- idiopathic pulmonary hemosiderosis [SNOMED Notion]
- pulmonary hemosiderosis [DO Concept]

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