Sacrococcygeal dysgenesis association

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 9
OrphanetNr: 1773
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:0000079) Abnormality of the urinary system Frequent [Orphanet] 88 / 7739
2
(HPO:0004374) Hemiplegia/hemiparesis Occasional [Orphanet] 158 / 7739
3
(HPO:0009800) Maternal diabetes Occasional [Orphanet] 14 / 7739
4
(HPO:0010305) Absence of the sacrum Very frequent [Orphanet] 17 / 7739
5
(HPO:0003298) Spina bifida occulta Occasional [Orphanet] 67 / 7739
6
(HPO:0005107) Abnormality of the sacrum Very frequent [Orphanet] 18 / 7739
7
(HPO:0002475) Myelomeningocele Occasional [Orphanet] 29 / 7739
8
(HPO:0003363) Abdominal situs inversus Occasional [Orphanet] 19 / 7739
9
(HPO:0004378) Abnormality of the anus Occasional [Orphanet] 34 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: