Pilonidal sinus

Symptom Information:

Symptom ID: HPO:0010769
Synonyms:
Pilonidal cyst [HPO:0010769]
Cyst - pilonidal [HPO:0010769]
Pilonidal sinus with abscess (disorder) [Orphanet:16660]
Pilonidal cyst with abscess (disorder) [Orphanet:16660]
Cyst - pilonidal (disorder) [Orphanet:16660]
Pilonidal Cyst [Orphanet:16660]
Pilonidal sinus with abscess [Orphanet:16660]
Pilonidal sinus [OMIM:Pilonidal sinus]
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]
Quality:
Cross references:
HPO:0010771 "Pilonidal abscess" [Orphanet:16660]
HPO:0000960 "Sacral dimple" [Orphanet:16660]
HPO:0010768 "Pilonidal cyst" [Orphanet:16660]
Orphanet:16660 "Sacral sinus/dimple" [Orphanet:16660]
OMIM: "Pilonidal sinus" [OMIM:Pilonidal sinus]
UMLS:C0031925 "Pilonidal Cyst" [Orphanet:16660]
UMLS:C0342988 "Pilonidal sinus with abscess" [Orphanet:16660]
Is a (Direct Parents):
Orphanet Abnormality of the sacrum
MedDRA Skin and subcutaneous tissue bacterial infections
Orphanet Sacral dimple
HPO         Sacrococcygeal pilonidal abnormality
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)
                         Pilonidal sinus(HPO:0010769)
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)
          Pilonidal sinus(HPO:0010769)
Database Frequency: 35 / 7739
Resource:

All diseases associated with this symptom:

17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
8p11.2 deletion syndrome (Orphanet:251066)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Bloom syndrome (Orphanet:125)
C syndrome (Orphanet:1308)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cartilage-hair hypoplasia (Orphanet:175)
Corpus callosum agenesis - double urinary collecting system (Orphanet:1492)
Craniofacial dyssynostosis (Orphanet:1516)
Craniosynostosis - fibular aplasia (Orphanet:1533)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Distal monosomy 3p (Orphanet:1620)
Distal trisomy 6p (Orphanet:1745)
Dubowitz syndrome (Orphanet:235)
Hand-foot-genital syndrome (Orphanet:2438)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
Isotretinoin syndrome (Orphanet:2305)
Lower limb deficiency - hypospadias (Orphanet:2487)
Mesomelic dwarfism, Nievergelt type (Orphanet:2633)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Miller-Dieker syndrome (Orphanet:531)
Monosomy 22q13 (Orphanet:48652)
PILONIDAL SINUS (OMIM:173000)
Peters-plus syndrome (Orphanet:709)
Phocomelia, Schinzel type (Orphanet:2879)
Posterior fusion of lumbosacral vertebrae - blepharoptosis (Orphanet:2064)
Stüve-Wiedemann syndrome (Orphanet:3206)
Teebi-Shaltout syndrome (Orphanet:3291)
Trisomy 9p (Orphanet:236)
Williams syndrome (Orphanet:904)
Wolf-Hirschhorn syndrome (Orphanet:280)
Xp22.3 microdeletion syndrome (Orphanet:1643)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)