Mild splenomegaly

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Mild splenomegaly" [OMIM:Mild splenomegaly]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT (OMIM:153670)
Sanfilippo syndrome type A (Orphanet:79269)
Sanfilippo syndrome type B (Orphanet:79270)
Sanfilippo syndrome type C (Orphanet:79271)
Sanfilippo syndrome type D (Orphanet:79272)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)