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Items: 2

1.

Tooth agenesis, selective, X-linked, 1

Any tooth agenesis in which the cause of the disease is a mutation in the EDA gene. [from MONDO]

MedGen UID:
410143
Concept ID:
C1970757
Disease or Syndrome
2.

Hypohidrotic X-linked ectodermal dysplasia

Hypohidrotic ectodermal dysplasia (HED) is characterized by hypotrichosis (sparseness of scalp and body hair), hypohidrosis (reduced ability to sweat), and hypodontia (congenital absence of teeth). The cardinal features of classic HED become obvious during childhood. The scalp hair is thin, lightly pigmented, and slow growing. Sweating, although present, is greatly deficient, leading to episodes of hyperthermia until the affected individual or family acquires experience with environmental modifications to control temperature. Only a few abnormally formed teeth erupt, at a later-than-average age. Physical growth and psychomotor development are otherwise within normal limits. Mild HED is characterized by mild manifestations of any or all the characteristic features. [from GeneReviews]

MedGen UID:
57890
Concept ID:
C0162359
Disease or Syndrome

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