Epidermoid cyst

Symptom Information:

Symptom ID: HPO:0200040
Synonyms:
Epidermal inclusion cyst [HPO:0200040]
EPIDERMOID CYSTS [HPO:0200040]
Skin cyst [HPO:0200040]
Epidermoid cysts [OMIM:Epidermoid cysts]
Epidermoid cysts (in 1/4 patients) [OMIM:Epidermoid cysts (in 1/4 patients)]
Epidermal cyst [MedDRA:10014983]
Epidermoid cyst [Orphanet:23680]
Epidermoid cyst (morphologic abnormality) [Orphanet:23680]
Sebaceous cyst (morphologic abnormality) [Orphanet:23680]
Keratinizing cyst (disorder) [Orphanet:23680]
Epidermoid cyst (disorder) [Orphanet:23680]
Epidermal inclusion cyst (morphologic abnormality) [Orphanet:23680]
Epidermoid cyst of skin (disorder) [Orphanet:23680]
Keratinizing cyst (morphologic abnormality) [Orphanet:23680]
Epithelial inclusion cyst (morphologic abnormality) [Orphanet:23680]
Epithelial inclusion cyst [Orphanet:23680]
Epithelial cyst [Orphanet:23680]
Skin tumors/lumps/epidermal cysts [Orphanet:23680]
Sebaceous cysts (buttocks and perineum) [OMIM:Sebaceous cysts (buttocks and perineum)]
Quality:
Cross references:
Orphanet:23680 "Skin tumors/lumps/epidermal cysts" [Orphanet:23680]
OMIM: "Epidermoid cysts" [OMIM:Epidermoid cysts]
OMIM: "Epidermoid cysts (in 1/4 patients)" [OMIM:Epidermoid cysts (in 1/4 patients)]
OMIM: "Sebaceous cysts (buttocks and perineum)" [OMIM:Sebaceous cysts (buttocks and perineum)]
UMLS:C0259770 "Epithelial inclusion cyst" [Orphanet:23680]
UMLS:C0014511 "Epithelial cyst" [Orphanet:23680]
Is a (Direct Parents):
HPO         Localized skin lesion
Orphanet Abnormality of the skin
Orphanet Neoplasm of the skin
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Localized skin lesion(HPO:0011355)
                Epidermoid cyst(HPO:0200040)
MedDRA:
Database Frequency: 35 / 7739
Resource:

All diseases associated with this symptom:

8q22.1 microdeletion syndrome (Orphanet:178303)
Attenuated familial adenomatous polyposis (Orphanet:220460)
Bloom syndrome (Orphanet:125)
Branchio-oculo-facial syndrome (Orphanet:1297)
Branchio-otic syndrome (Orphanet:52429)
Campomelia, Cumming type (Orphanet:1318)
Campomelic dysplasia (Orphanet:140)
Carney complex (Orphanet:1359)
Cleft palate - large ears - small head (Orphanet:2013)
Desmoid tumor (Orphanet:873)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Facial ectodermal dysplasia (Orphanet:1807)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Fuhrmann syndrome (Orphanet:2854)
Gorlin syndrome (Orphanet:377)
Grant syndrome (Orphanet:2097)
Hypophosphatasia (Orphanet:436)
Kyphomelic dysplasia (Orphanet:1801)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 (OMIM:614114)
Macrostomia - preauricular tags - external ophthalmoplegia (Orphanet:83619)
Mesomelic dwarfism - cleft palate - camptodactyly (Orphanet:2631)
Mesomelic dwarfism, Nievergelt type (Orphanet:2633)
Mesomelic dwarfism, Reinhardt-Pfeiffer type (Orphanet:2634)
Multiple benign circumferential skin creases on limbs (Orphanet:2505)
Neurogenic arthrogryposis multiplex congenita (Orphanet:1143)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Oculocerebrorenal syndrome (Orphanet:534)
PACHYONYCHIA CONGENITA 2 (OMIM:167210)
PACHYONYCHIA CONGENITA 3 (OMIM:615726)
Paternal 20q13.2q13.3 microdeletion syndrome (Orphanet:261304)
Pelvic dysplasia - arthrogryposis of lower limbs (Orphanet:2840)
Pituitary dermoid and epidermoid cysts (Orphanet:91351)
Progeroid syndrome, Petty type (Orphanet:2963)
Syngnathia multiple anomalies (Orphanet:3262)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)