Phenotypes for disease #03795 (ECTD11A (dysplasia, ectodermal, type 11A, hypohidrotic/hair/tooth, autosomal dominant (ECTD11A)), OMIM:614940)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000034020 very thin, brittle, sparse or even absent hair, reduced sweating ability, dental panoramic radiographs confirmed absence considerable number permanent teeth (six upper jaw, eight lower jaw), bilateral amazia (unilateral amazia in mother, bilateral mature ovarian teratomas containing hair, sebaceous and sweat glands - ECTD11A Familial, autosomal dominant 16y - - - - Johan den Dunnen 00043753
0000044561 sparse hair (HP:0008070), reduced number of teeth (HP:0009804), hypohidrosis (HP:000966), dry skin (HP:0000958), abnormal nails (HP:0001597), palmoplantar keratoderma (HP:0000982) - - Familial, autosomal dominant 11y - - - - Johan den Dunnen 00057908
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