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Diseases

Ectodermal Dysplasia 11B, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive

ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Ectodermal Dysplasia 11B, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive
Standard Disease Name
ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
No data
OMIM ID
No data
UMLS ID
C1332242
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A rare, aggressive malignant tumor that originates from an odontogenic cyst in the maxillomandibular region. It combines the histologic features of an ameloblastoma and carcinoma.
Related

Direct relations and traceable candidates grouped by relation type.