Autosomal dominant contiguous gene syndrome

Symptom Information:

Symptom ID: HPO:0001452
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Autosomal dominant inheritance
HPO         Contiguous gene syndrome
Is a (Whole tree): HPO:
All(HPO:0000001)
    Mode of inheritance(HPO:0000005)
       Contiguous gene syndrome(HPO:0001466)
          Autosomal dominant contiguous gene syndrome(HPO:0001452)
       Autosomal dominant inheritance(HPO:0000006)
          Autosomal dominant contiguous gene syndrome(HPO:0001452)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

CHROMOSOME 8q12.1-q21.2 DELETION SYNDROME (OMIM:600257)
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality (Orphanet:86841)
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion (Orphanet:353281)
Waardenburg syndrome (Orphanet:3440)