Phenotypes for disease #00815 (MRD7 (mental retardation, autosomal dominant, type 7 (MRD-7)), OMIM:614104)

10 entries on 1 page. Showing entries 1 - 10.
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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     
0000044552 Microcephaly HP:0000252 - - Familial, autosomal dominant - - - - - - Birgit Sikkema-Raddatz 00057262
0000060557 Mental retardation, autosomal dominant 7 (OMIM:614104) - - Isolated (sporadic) - - - - - - Daniel Trujillano 00080988
0000070595 moderate IDD, intractable absence epilepsy, acquired microcephaly, failure to thrive; GLUT-DS like phenotype (hypoglycorrhagia, low CSF:serum glucose ratio) - - Familial, autosomal dominant - - - - - - Johan den Dunnen 00092260
0000275385 Abnormal cry, High-pitched cry, Microcephaly, High palate, Thin vermilion border, Abnormal lip morphology, Retrognathia, Failure to thrive, Decreased body weight, Retinal dysplasia, Abnormal retinal morphology, Global developmental delay 01mo - Isolated (sporadic) - - - - - - Andreas Laner 00381536
0000283621 Abnormal cry, High-pitched cry, Microcephaly, High palate, Thin vermilion border, Abnormal lip morphology, Retrognathia, Failure to thrive, Decreased body weight, Retinal dysplasia, Abnormal retinal morphology, Global developmental delay - - Familial, autosomal dominant - - - - - - Andreas Laner 00390083
0000308144 Neurodevelopmental delay, Delayed CNS myelination, Cataract, Microcephaly - - Isolated (sporadic) - 01y - - - - Andreas Laner 00416379
0000308361 brain magnetic resonance imaging: wide peripheral liquor spaces; additional clinical featureslow birth weight, brachycephaly, hypertonia, severe developmental delay (consanguineous parents) - Autosomal dominant mental retardation 7 [MIM 614104] Familial, autosomal dominant 2y - - - - - LOVD 00416851
0000324083 moderate intellectual disability - - Isolated (sporadic) - - - - - - Marketa Wayhelova 00433660
0000325531 Global developmental delay, Delayed speech and language development, Motor delay, Failure to thrive, Abnormal aortic arch morphology - - Isolated (sporadic) 02y - - - - - Andreas Laner 00435334
0000342124 Focal-onset seizure, Febrile seizure (within the age range of 3 months to 6 years), Microcephaly, Neurodevelopmental delay, Motor delay, Delayed speech and language development - - Isolated (sporadic) 02y - - - - - Andreas Laner 00453460
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