Phenotypes for disease #02385 (TIDAND (T-cell immunodeficiency, congenital alopecia and nail dystrophy), OMIM:601705)

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000122639 born with complete absence scalp hair /eyebrows / eyelashes; dystrophic nails, no thymic shadow on X-ray; striking impairment T-cell function (1 sister died 12m, other sister received bone marrow transplant) - - Familial, autosomal recessive - - - - - Johan den Dunnen 00150235
0000122640 see paper, ..., born at term, nail dystrophy, no hair, infection - - Familial, autosomal recessive - - - - - Johan den Dunnen 00150236
0000122641 see paper; ..., born at term, no hair, dystrophic nails, respiratory distress - - Familial, autosomal recessive - - - - - Johan den Dunnen 00150237
0000122642 see paper; ..., diffuse, eczematous rash progressed in 2w to erythroderma, severe diarrhea, congenital alopecia, T cell immunodeficiency - - Familial, autosomal recessive - - 00y01m diffuse, eczematous rash - Johan den Dunnen 00150238
0000303398 Muscular dystrophy - - Familial, autosomal recessive - - - - - Ponghatai Damrongphol 00411322
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