Phenotypes for disease #00801 (MRT13 (mental retardation, autosomal recessive, type 13), OMIM:613192)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Birth_Details     

Protein     

Owner     

Individual ID     
0000060373 Mental retardation, autosomal recessive 13 (OMIM:613192) - - Familial, autosomal recessive - - - - - - Daniel Trujillano 00080804
0000083799 Intellectual disability (HP:0001249); truncal obesity (HP:0001956); no neutropenia (HP:0001875) - - Familial, autosomal recessive 30y - 00y06m - - - Dominique Germain 00105899
0000304318 Microcephaly, Cerebellar vermis hypoplasia, Partial agenesis of the corpus callosum, Short stature, Pain insensitivity, Neurodevelopmental delay, Posterior atrophy of corpus callosum, Self-injurious behavior - - Familial, autosomal recessive 10y - - - - - Andreas Laner 00412313
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