Pilonidal sinus
Symptom Information:
Symptom ID: | HPO:0010769 | |||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) |
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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) |