Secondary intestinal lymphangiectasia

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 16
OrphanetNr: 90363
OMIM Id:
ICD-10: I89.0
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Intestinal lymphangiectasia
 -Rare circulatory system disease
 -Rare developmental defect during embryogenesis
 -Rare gastroenterologic disease
 -Rare genetic disease
 -Rare skin disease

Symptom Information: Sort by abundance 

1
 (HPO:0100769) Synovitis Occasional [Orphanet] 86 / 7739
2
 (HPO:0002037) Inflammation of the large intestine Occasional [Orphanet] 25 / 7739
3
 (HPO:0002024) Malabsorption Very frequent [Orphanet] 142 / 7739
4
 (HPO:0001541) Ascites Occasional [Orphanet] 94 / 7739
5
 (HPO:0001072) Thickened skin Occasional [Orphanet] 87 / 7739
6
 (HPO:0200042) Skin ulcer Frequent [Orphanet] 138 / 7739
7
 (HPO:0200037) Skin vesicle Frequent [Orphanet] 102 / 7739
8
 (HPO:0001888) Lymphopenia Very frequent [Orphanet] 43 / 7739
9
 (HPO:0004377) Hematological neoplasm Occasional [Orphanet] 12 / 7739
10
 (HPO:0010741) Edema of the lower limbs Very frequent [Orphanet] 34 / 7739
11
 (HPO:0002901) Hypocalcemia Frequent [Orphanet] 56 / 7739
12
 (HPO:0001004) Lymphedema Occasional [Orphanet] 62 / 7739
13
 (HPO:0002103) Abnormality of the pleura Occasional [Orphanet] 58 / 7739
14
 (HPO:0002664) Neoplasm Occasional [Orphanet] 111 / 7739
15
 (HPO:0002960) Autoimmunity Occasional [Orphanet] 78 / 7739
16
 (HPO:0100763) Abnormality of the lymphatic system Very frequent [Orphanet] 18 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: