Idiopathic pulmonary hemosiderosis

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 7
OrphanetNr: 99931
OMIM Id: 178550
235500
ICD-10: E83.1+
J99.8*
UMLs: C0020807
MeSH: C536281
MedDRA:
Snomed: 40527005

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset: Childhood
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Primary interstitial lung disease in childhood and adulthood
 -Rare respiratory disease

Symptom Information: Sort by abundance 

1
 (HPO:0006535) Recurrent intrapulmonary hemorrhage 3 / 7739
2
 (HPO:0001891) Iron deficiency anemia 22 / 7739
3
 (HPO:0002093) Respiratory insufficiency 410 / 7739
4
 (HPO:0002105) Hemoptysis 30 / 7739
5
 (HPO:0002206) Pulmonary fibrosis 51 / 7739
6
 (HPO:0005828) Transient pulmonary infiltrates 2 / 7739
7
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: