Brachydactyly-mesomelia-intellectual disability-heart defects syndrome

Brachydactyly-mesomelia-intellectual disability-heart defects syndrome is a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, intellectual disability, thin habitus with narrow shoulders, mesomelic shortness of the arms, craniofacial dysmorphism (e.g. long lower face, maxillary hypoplasia, beak nose, short columella, prognathia, high arched palate, obtuse mandibular angle), brachydactyly (mostly involving middle phalanges) and cardiovascular anomalies (i.e. aortic root dilatation, mitral valve prolapse).



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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
        

Phenotype(s) retrieved from Orphanet

    Total: 11

HPO ID Term Frequency
HP:0000174 Abnormal palate morphology Very frequent (99-80%)
HP:0000347 Micrognathia Very frequent (99-80%)
HP:0000444 Convex nasal ridge Very frequent (99-80%)
HP:0001156 Brachydactyly Very frequent (99-80%)
HP:0001633 Abnormal mitral valve morphology Very frequent (99-80%)
HP:0003027 Mesomelia Very frequent (99-80%)
HP:0003043 Abnormality of the shoulder Very frequent (99-80%)
HP:0004299 Hernia of the abdominal wall Very frequent (99-80%)
HP:0009804 Reduced number of teeth Very frequent (99-80%)
HP:0100543 Cognitive impairment Very frequent (99-80%)
HP:0100818 Long thorax Very frequent (99-80%)


Phenotype(s) retrieved from case reports

    Total: 0

HPO ID Term # of case reports


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID