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

Official abbreviation MRD23
Name mental retardation, autosomal dominant, type 23 (MRD-23)
OMIM ID 615761
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene SETD5
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00377162 181846 - - M no Germany - - - - - MRD23 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 SETD5 SETD5 1 1 Andreas Laner
00416299 203952 - - M no Russia - - - - - MRD23 Hypotonia, Failure to thrive, Delayed gross motor development, Decreased body weight SETD5 SETD5 1 1 Andreas Laner
00442607 274684 - - F no Germany - - - - - MRD23 Microcephaly, Autism, Intellectual disability, Atrial septal defect, Visual impairment, Hypothyroidism, Disinhibition, Reduced eye contact SETD5 SETD5 1 1 Andreas Laner
00453815 304406 - - M no Ukraine - - - - - MRD23 Absent speech, Neurodevelopmental delay, Motor delay SETD5 SETD5 1 1 Andreas Laner
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