Absence of the sacrum

Symptom Information:

Symptom ID: HPO:0010305
Synonyms:
Absent sacrum [HPO:0010305]
Sacrococcygeal agenesis [Orphanet:16690]
Absent sacrum [OMIM:Absent sacrum]
Sacrococcyx agenesis [Orphanet:16690]
Quality:
Cross references:
Orphanet:16690 "Sacrococcyx agenesis" [Orphanet:16690]
OMIM: "Absent sacrum" [OMIM:Absent sacrum]
Is a (Direct Parents):
Orphanet Abnormality of the sacrum
HPO         Aplasia/Hypoplasia of the sacrum
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving the vertebral column(HPO:0008518)
                      Aplasia/Hypoplasia of the sacrum(HPO:0008517)
                         Absence of the sacrum(HPO:0010305)
                Abnormality of the vertebral column(HPO:0000925)
                   Abnormality of the sacrum(HPO:0005107)
                      Aplasia/Hypoplasia of the sacrum(HPO:0008517)
                         Absence of the sacrum(HPO:0010305)
                   Aplasia/Hypoplasia involving the vertebral column(HPO:0008518)
                      Aplasia/Hypoplasia of the sacrum(HPO:0008517)
                         Absence of the sacrum(HPO:0010305)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving the vertebral column(HPO:0008518)
                      Aplasia/Hypoplasia of the sacrum(HPO:0008517)
                         Absence of the sacrum(HPO:0010305)
MedDRA:
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

Anophthalmia plus syndrome (Orphanet:1104)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
Caudal regression sequence (Orphanet:3027)
Cloacal exstrophy (Orphanet:93929)
Currarino triad (Orphanet:1552)
Diabetic embryopathy (Orphanet:1926)
Exstrophy-epispadias complex (Orphanet:322)
Familial caudal dysgenesis (Orphanet:1768)
Holoprosencephaly - caudal dysgenesis (Orphanet:2165)
Limb body wall complex (Orphanet:2369)
Multiple epiphyseal dysplasia (Orphanet:251)
Renal dysplasia - megalocystis - sirenomelia (Orphanet:1850)
Sacrococcygeal dysgenesis association (Orphanet:1773)
Sirenomelia (Orphanet:3169)
Splenogonadal fusion - limb defects - micrognathia (Orphanet:2063)
VACTERL with hydrocephalus (Orphanet:3412)
Verloove Vanhorick-Brubakk syndrome (Orphanet:3429)