Phenotypes for disease #03971 (MRD21 (mental retardation, autosomal dominant, type 21 (MRD-21)), OMIM:615502)

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     
0000242419 ultrasound abnormality: fetal retrognathia, microcephaly prenatal - Unknown - - - - - - Andreas Laner 00320443
0000274651 DD; ID; microcephaly; short stature (Neurological) - Mental retardation type 21 Familial - - - - - - LOVD 00380798
0000325526 microcephaly, cleft palate, fetal retardation mental retardation MRD21 Isolated (sporadic) - - - - - - Tuan Nguyen 00435330
0000335808 Small for gestational age, Moderate global developmental delay, Protruding ear, Facial asymmetry, Cranial asymmetry, Premature birth - - Isolated (sporadic) 00y08m - - - - - Andreas Laner 00446608
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