Transverse limb deficiency - hemangioma

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 2
OrphanetNr: 2486
OMIM Id:
ICD-10: D18.0
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: Vascular tumor
 -Rare circulatory system disease
 -Rare developmental defect during embryogenesis

Symptom Information: Sort by abundance 

1
(HPO:0002983) Micromelia Very frequent [Orphanet] 130 / 7739
2
(HPO:0001048) Cavernous hemangioma Very frequent [Orphanet] 28 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: