Phenotypes for disease #05555 (NEDIDHA (neurodevelopmental disorder, impaired intellectual development, hypotonia, and ataxia (NEDIDHA)), OMIM:618292)

10 entries on 1 page. Showing entries 1 - 10.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000179275 Developmental delay - With sick sinus syndrome Familial, autosomal dominant - - 00y03m muscle weakness Kazuhiro Iwama 00238978
0000280170 - - HP:0011342; HP:0002069; HP:0002066; HP:0008619; HP:0000505 Familial, autosomal recessive - - 00y00m01d - Simone Seiffert 00385786
0000280171 - - HP:0011342; HP:0002066; HP:0008619 Familial, autosomal recessive - - 01y - Simone Seiffert 00385787
0000280172 - - HP:0011342; HP:0010535; HP:0000338; HP:0000488; HP:0011476; HP:0002066; HP:0002650; HP:0001761 Familial, autosomal recessive - - 08y - Simone Seiffert 00385788
0000280173 - - HP:0011170; HP:0002069; HP:0002133; HP:0011147 Familial, autosomal recessive - - 06y - Simone Seiffert 00385790
0000280174 - - HP:0001263; HP:0002069; HP:0012469; HP:0001252; HP:0002521; HP:0000639;HP:0000505; HP:0001385 Familial, autosomal recessive - - 00y06m - Simone Seiffert 00385821
0000280175 - - HP:0001263; HP:0001249; HP:0011153; HP:0002069; HP:0002510; HP:0000648; HP:0000218; HP:0002650; HP:0000252; HP:0006970; HP:0002079 Familial, autosomal recessive - - 00y05m - Simone Seiffert 00385822
0000280176 - - HP:0001256; HP:0030799; HP:0009733 Familial, autosomal recessive - - - 3m Simone Seiffert 00385823
0000280177 - - HP:0002342; HP:0001252; HP:0000639 Familial, autosomal recessive - - - 3m-4m Simone Seiffert 00385824
0000280178 - - HP:0001263; HP:0001249; HP:0001250; HP:0001252; HP:0002066; HP:0000365; HP:0000505; HP:0001488; HP:0000218 Familial, autosomal recessive - - - 2m Simone Seiffert 00385825
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