Phenotypes for disease #01298 (ECTD10A (dysplasia, ectodermal, type 10A, hypohidrotic/hair/nail, autosomal dominant (ECTD10A)), OMIM:129490)

9 entries on 1 page. Showing entries 1 - 9.
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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     
0000044546 sparse hair (HP:0008070), reduced number of teeth (HP:0009804), hypohidrosis (HP:000966), facial dysmorphism (HP:0001999) - - Familial, autosomal dominant - - - - - Johan den Dunnen 00057899
0000044555 sparse hair (HP:0008070), reduced number of teeth (HP:0009804), hypohidrosis (HP:000966), facial dysmorphism (HP:0001999) - - Familial, autosomal dominant 17y - - - - Johan den Dunnen 00057900
0000044556 sparse hair (HP:0008070), reduced number of teeth (HP:0009804), hypohidrosis (HP:000966), dry skin (HP:0000958) - - Familial, autosomal dominant 34y - - - - Johan den Dunnen 00057901
0000044558 sparse hair (HP:0008070), reduced number of teeth (HP:0009804), hypohidrosis (HP:000966); autosomal dominant case - - Isolated (sporadic) 37y - - - - Johan den Dunnen 00057903
0000044559 sparse hair (HP:0008070), reduced number of teeth (HP:0009804), hypohidrosis (HP:000966), dry skin (HP:0000958), eczema (HP:0000964) - - Familial, autosomal dominant 10y - - - - Johan den Dunnen 00057905
0000044560 sparse hair (HP:0008070), reduced number of teeth (HP:0009804), hypohidrosis (HP:000966) - - Familial, autosomal dominant 06y - - - - Johan den Dunnen 00057906
0000045119 hypohidrotic ectodermal dysplasia - - Familial, autosomal dominant - - - - - Sigrun Maier-Wohlfart 00058499
0000045120 hypohidrotic ectodermal dysplasia - - Familial, autosomal dominant - - - - - Sigrun Maier-Wohlfart 00058500
0000227115 hypohidrotic ectodermal dysplasia hypohidrotic ectodermal dysplasia ECTD10A Familial, X-linked dominant - - - - - Sigrun Maier-Wohlfart 00299797
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