Phenotypes for disease #00017 (MRXS10 (mental retardation, X-linked syndromic, type 10 (MRXS-10)), OMIM:300220)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Enzyme/Activity     

Protein     

Age/Diagnosis     

Owner     

Individual ID     
0000000852 - Familial - - - - ascertainment clinical presentation; mild mental retardation, choreoathetosis, abnormal behavior almost normal MHBD activity, amounting to 85% of the level in controls - - Division of Human Genetics, Innsbruck 00001698
0000000853 - Unknown - - - - ascertainment clinical presentation; mental retardation - - - Division of Human Genetics, Innsbruck 00001699
0000002031 - Familial, X-linked recessive - - - - lissencephaly, agenesis corpus callosum - - - Johan den Dunnen 00003191
0000025727 - Familial, X-linked recessive - - - - mental retardation, different syndromes - - - Claus Lenski 00029716
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