Phenotypes for disease #04076 (MRD23 (mental retardation, autosomal dominant, type 23 (MRD-23)), OMIM:615761)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000272320 Functional abnormality of the bladder, Nocturia, Abnormal eyebrow morphology, Synophrys, Short attention span, Hyperactivity, Global developmental delay, Neurological speech impairment, Facial hypertrichosis, Febrile seizure (within the age range of 3 months to 6 years), Attention deficit hyperactivity disorder, Neurodevelopmental delay, Stuttering, Seizure precipitated by febrile infection - 9y Familial, autosomal dominant - - - - - - Andreas Laner 00377162
0000308066 Hypotonia, Failure to thrive, Delayed gross motor development, Decreased body weight - - Unknown 02y - - - - - Andreas Laner 00416299
0000331954 Microcephaly, Autism, Intellectual disability, Atrial septal defect, Visual impairment, Hypothyroidism, Disinhibition, Reduced eye contact - - Isolated (sporadic) 16y - - - - - Andreas Laner 00442607
0000342470 Absent speech, Neurodevelopmental delay, Motor delay - - Unknown 04y - - - - - Andreas Laner 00453815
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