Diprosopia

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 9
OrphanetNr: 1681
OMIM Id:
ICD-10:
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: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0000366) Abnormality of the nose Very frequent [Orphanet] 56 / 7739
2
 (HPO:0000271) Abnormality of the face Very frequent [Orphanet] 108 / 7739
3
 (HPO:0000174) Abnormality of the palate Very frequent [Orphanet] 298 / 7739
4
 (HPO:0000204) Cleft upper lip Frequent [Orphanet] 193 / 7739
5
 (HPO:0000478) Abnormality of the eye Very frequent [Orphanet] 126 / 7739
6
 (HPO:0000510) Rod-cone dystrophy Very frequent [Orphanet] 266 / 7739
7
 (HPO:0000356) Abnormality of the outer ear Very frequent [Orphanet] 85 / 7739
8
 (HPO:0004760) Congenital septal defect Very frequent [Orphanet] 69 / 7739
9
 (HPO:0002323) Anencephaly Very frequent [Orphanet] 28 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: