Contiguous gene syndrome

Symptom Information:

Symptom ID: HPO:0001466
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Mode of inheritance
Is a (Whole tree): HPO:
All(HPO:0000001)
    Mode of inheritance(HPO:0000005)
       Contiguous gene syndrome(HPO:0001466)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
Choroideremia - deafness - obesity (Orphanet:1435)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Koolen-De Vries syndrome (Orphanet:96169)
Miller-Dieker syndrome (Orphanet:531)
Potocki-Shaffer syndrome (Orphanet:52022)
WAGR syndrome (Orphanet:893)