Disease #01004 (SMS (Smith-Magenis syndrome (SMS)), OMIM:182290)

Official abbreviation SMS
Name Smith-Magenis syndrome (SMS)
OMIM ID 182290
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Isolated Cases (Sporadic)
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene RAI1
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

6 entries on 1 page. Showing entries 1 - 6.
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00163511 - PubMed: Liburd et al., 2001 proband - - - - - - - - SMS Smith-Magenis Syndrome presenting hearing loss MYO15A MYO15A 2 1 Anne-Françoise Roux
00409864 196579 - - M ? Turkey - - - - - SMS Autism, Autistic behavior, Attention deficit hyperactivity disorder, Myopia, Hypertension, Obesity, Synophrys, Sensorineural hearing impairment, Delayed speech and language development, Abnormality of pain sensation, Abnormal aggressive, impulsive or violent behavior, Self-injurious behavior, Short toe, Sleep disturbance, Brachydactyly RAI1 RAI1 1 1 Andreas Laner
00431213 FamPatII2 PubMed: Adams 2014 sister F - - Jew-Ashkenazi - - - - PCKDC, SMS episodic fasting hypoglycemia, lactic acidemia, see paper; ..., obesity, brachydactyly, developmental delay, cognitive impairment, behavioral outbursts, sleep disruption, facial appearance - PCK1, RAI1 2 1 Johan den Dunnen
00433658 - - - - - - - - - - - SMS ID, behavioural abnormalities, obesity, visual and hearing defect - RAI1 1 1 Marketa Wayhelova
00434050 - - - - - - - - - - - SMS growth restriction, microcephaly, developmental delay, hearing defect, ichtyosis vulgaris - RAI1 1 1 Marketa Wayhelova
00435356 264393 - - M no Germany - - - - - SMS Neurodevelopmental delay, Short attention span, Hyperactivity RAI1 RAI1 1 1 Andreas Laner
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