DiseaseID 3793

毛发囊肿

disease

MSH2017_2016_08_12:Intradermal or subcutaneous saclike structure, the wall of which is stratified epithelium containing keratohyalin granules.|HPO2016_07_04:The presence of one or more cysts of the skin. [HPO:skoehler]

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Disease: 1Symptom: 11Target: 12Links: 23
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Record Fields

Scalar fields from the final disease record.

Disease Id
3793
Core Entity Id
60042
Source Entity Count
1
Preferred Name
Pilar Cyst
Name Cn
毛发囊肿
Name Pinyin
Mao Fa Nang Zhong
Name En
Pilar Cyst
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Anatomical Abnormality
Disgenet Type
disease
Mesh Class
Neoplasms
Do Class
disease of cellular proliferation
Hpo Class
Abnormality of the integument
Mesh Class Name
Neoplasms
Hpo Class Name
Abnormality of the integument
Do Class Name
disease of cellular proliferation
Disease Definition
MSH2017_2016_08_12:Intradermal or subcutaneous saclike structure, the wall of which is stratified epithelium containing keratohyalin granules.|HPO2016_07_04:The presence of one or more cysts of the skin. [HPO:skoehler]
Version
v2
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Pilar Cyst
Role
preferred
Name
Dermoid Cyst
Role
preferred
Name
Epithelial Cyst
Role
preferred
Name
TRICHILEMMAL CYST 1
Role
preferred
Name
Cyst, Pilar
Role
alias
Name
Epidermal Cyst
Role
alias
Name
Epidermal Inclusion Cyst
Role
alias
Name
Epidermoid Cyst
Role
alias
Name
Epidermoid Cysts
Role
alias
Name
Infundibular Cyst
Role
alias
Name
Keratin Cyst
Role
alias
Name
Sebaceous Cyst
Role
alias
Name
Skin Cyst
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Hpo
HP:0025247HP:0200040
Herb
HBDIS000769HBDIS000949HBDIS003433HBDIS018126
Me Sh
D003884D004814
Omim
131600609649
Umls
C0011649C0014511
Icd10
K09.8L72.0L72.3
Sym Map
SMDE07832SMDE08442
Do Class
DOID:14566
Dis Ge Net
C0011649C0014511C0086809C1864801
Umls Sty
T047T190T191
Hpo Class
HP:0001574
Me Sh Class
C04
Tcmbank Disease
161481763428165301639272
Itcmdb Generated
ITX-DISEASE-B40BE4AAD13D

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Do Class Name
disease of cellular proliferation
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of the integument
Do Disease Class
disease of cellular proliferation
Hpo Disease Class
Abnormality of the integument
Umls Disease Type
Anatomical AbnormalityDisease or SyndromeNeoplastic Process
Disease Definition
MSH2017_2016_08_12:Intradermal or subcutaneous saclike structure, the wall of which is stratified epithelium containing keratohyalin granules.|HPO2016_07_04:The presence of one or more cysts of the skin. [HPO:skoehler]NCI2016_NICHD_1602D:A benign hamartomatous tumor that possesses various epidermal derivatives and is due to sequestration of skin along the lines of embryonic closure. In neonates, it is most commonly congenital and located in the subcutaneous tissues of the head, neck, or trunk.|NCI2016_NCI-GLOSS_1602D:A type of benign (not cancer) germ cell tumor (type of tumor that begins in the cells that give rise to sperm or eggs) that often contains several different types of tissue such as hair, muscle, and bone.|NCI2016_CDISC_1602D:A benign neoplasm comprised of a cyst, lined by mature epidermis-like tissue with dermal appendages.|NCI2016_02D:A mature teratoma characterized by the presence of a cyst which is lined by mature tissue resembling the epidermis and the epidermal appendages. It occurs in the ovary, testis, and extragonadal sites including central nervous system and skin.|MSH2017_2016_08_12:A tumor consisting of displaced ectodermal structures along the lines of embryonic fusion, the wall being formed of epithelium-lined connective tissue, including skin appendages, and containing keratin, sebum, and hair. (Stedman, 25th ed)|CHV2011_02:A benign tumor resulting from abnormal embryonic development|CHV2011_02:A benign tumor resulting from abnormal embryonic development|CHV2011_02:A benign tumor resulting from abnormal embryonic development|CHV2011_02:A benign tumor resulting from abnormal embryonic development|CHV2011_02:A benign tumor resulting from abnormal embryonic development|CHV2011_02:A benign tumor resulting from abnormal embryonic development|CHV2011_02:A benign tumor resulting from abnormal embryonic development|CHV2011_02:A benign tumor resulting from abnormal embryonic development|CHV2011_02:A benign tumor resulting from abnormal embryonic development
Me Sh Disease Class
Neoplasms
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Neoplasms
Umls Semantic Type Name
Anatomical AbnormalityDisease or SyndromeNeoplastic Process