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

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description A disorder due to abnormal development of two or more ectodermal structures, and characterized by sparse hair (atrichosis or hypotrichosis), abnormal or missing teeth and the inability to sweat due to the absence of sweat glands.
Mondo Term and Equivalent IDs
MONDO:0013983:  ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive
DOID:0111654: 
UMLS:C3539920: