Disease #04619 (WHSUS;MRD37 (White-Sutton syndrome (WHSUS, mental retardation, autosomal dominant, type 37 (MRD-37))), OMIM:616364)

Official abbreviation WHSUS;MRD37
Name White-Sutton syndrome (WHSUS, mental retardation, autosomal dominant, type 37 (MRD-37))
OMIM ID 616364
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene POGZ
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00409821 195198 - - M no Germany - - - - - WHSUS;MRD37 Delayed speech and language development, Cryptorchidism, Mild microcephaly, Brachycephaly, Gait disturbance POGZ POGZ 1 1 Andreas Laner
00448489 286202 - - M no Germany - - - - - WHSUS;MRD37 Short stature, Neurodevelopmental delay, Impulsivity, Delayed speech and language development, Impaired social interactions, Enuresis, Self-injurious behavior, Aggressive behavior, Abnormal eating behavior, Smooth philtrum, Thin upper lip vermilion POGZ POGZ 1 1 Andreas Laner
00458062 311870 - - F no Germany - - - - - WHSUS;MRD37 Neurodevelopmental delay, Intellectual disability, Intellectual disability, mild, Atypical behavior, Obesity, Amblyopia, Polyphagia, Self-injurious behavior POGZ POGZ 1 1 Andreas Laner
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