Disease #06115 (SSMG;SRMMD (short stature-micrognathia syndrome), OMIM:617164)

Official abbreviation SSMG;SRMMD
Name short stature-micrognathia syndrome
OMIM ID 617164
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ARCN1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2025-02-28 13:05:45 +01:00 (CET)


Individuals

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00464283 323471 - - M no Germany - - - - - SSMG;SRMMD small for gestational age, short stature, pectus excavatum, motor delay, premature birth, intrauterine growth retardation, failure to thrive ARCN1 ARCN1 1 1 Andreas Laner
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