Sacral dimple

Symptom Information:

Symptom ID: HPO:0000960
Synonyms:
Pilonidal dimple [HPO:0000960]
Pilonidal sinus [Orphanet:16660]
Pilonidal sinus with abscess (disorder) [Orphanet:16660]
Pilonidal cyst with abscess (disorder) [Orphanet:16660]
Cyst - pilonidal (disorder) [Orphanet:16660]
Sacral dimples (finding) [Orphanet:16660]
Sacral dimple (finding) [Orphanet:16660]
Pilonidal Cyst [Orphanet:16660]
Pilonidal sinus with abscess [Orphanet:16660]
Sacral dimples [Orphanet:16660]
Pilonidal dimple [OMIM:Pilonidal dimple]
Sacral dimple [OMIM:Sacral dimple]
Sacral sinus/dimple [Orphanet:16660]
Pilonidal cyst with abscess [Orphanet:16660]
Pilonidal cyst [Orphanet:16660]
Pilonidal cyst [MedDRA:10035043]
Abscess pilonidal [MedDRA:10035043]
Pilonidal abscess [MedDRA:10035043]
Pilonidal cyst with abscess [MedDRA:10035043]
Pilonidal cyst without mention of abscess [MedDRA:10035043]
Pilonidal sinus infected [MedDRA:10035043]
Pilonidal cyst pain [MedDRA:10035043]
Pilonidal sinus [MedDRA:10035043]
Sacral dimple (in some patients) [OMIM:Sacral dimple (in some patients)]
Quality:
Cross references:
HPO:0010771 "Pilonidal abscess" [Orphanet:16660]
HPO:0010769 "Pilonidal sinus" [Orphanet:16660]
HPO:0010768 "Pilonidal cyst" [Orphanet:16660]
Orphanet:16660 "Sacral sinus/dimple" [Orphanet:16660]
OMIM: "Pilonidal dimple" [OMIM:Pilonidal dimple]
OMIM: "Sacral dimple" [OMIM:Sacral dimple]
OMIM: "Sacral dimple (in some patients)" [OMIM:Sacral dimple (in some patients)]
UMLS:C0031925 "Pilonidal Cyst" [Orphanet:16660]
UMLS:C0342988 "Pilonidal sinus with abscess" [Orphanet:16660]
UMLS:C0426848 "Sacral dimples" [Orphanet:16660]
Is a (Direct Parents):
HPO         Skin dimples
Orphanet Abnormality of the sacrum
HPO         Sacrococcygeal pilonidal abnormality
MedDRA Skin and subcutaneous tissue bacterial infections
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)
                Abnormality of the vertebral column(HPO:0000925)
                   Abnormality of the sacrum(HPO:0005107)
                      Sacrococcygeal pilonidal abnormality(HPO:0010767)
                         Sacral dimple(HPO:0000960)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Localized skin lesion(HPO:0011355)
                Skin dimples(HPO:0010781)
                   Sacral dimple(HPO:0000960)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin and subcutaneous tissue infections and infestations(MedDRA:10040792)
       Skin and subcutaneous tissue bacterial infections(MedDRA:10040788)
          Sacral dimple(HPO:0000960)
Database Frequency: 29 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
3MC SYNDROME 1 (OMIM:257920)
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA (OMIM:613623)
Bloom syndrome (Orphanet:125)
Bohring-Opitz syndrome (Orphanet:97297)
CARPENTER SYNDROME 1 (OMIM:201000)
COFFIN-SIRIS SYNDROME (OMIM:135900)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Carpenter syndrome (Orphanet:65759)
Cataract-congenital heart disease-neural tube defect syndrome (Orphanet:314993)
Cerebro-facio-articular syndrome (Orphanet:314679)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Coffin-Siris syndrome (Orphanet:1465)
DK1-CDG (Orphanet:91131)
Distal monosomy 3p (Orphanet:1620)
Dubowitz syndrome (Orphanet:235)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Intellectual deficit, Birk-Barel type (Orphanet:166108)
Koolen-De Vries syndrome (Orphanet:96169)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 24 (OMIM:615828)
Meckel syndrome, type 10 (OMIM:614175)
Miller-Dieker syndrome (Orphanet:531)
Monosomy 22q13 (Orphanet:48652)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
TETRAAMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES (OMIM:273390)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
Wiedemann-Steiner syndrome (Orphanet:319182)
Wolf-Hirschhorn syndrome (Orphanet:280)