Disease #06697 (FMD2 (Frontometaphyseal dysplasia 2), OMIM:617137)

Official abbreviation FMD2
Name Frontometaphyseal dysplasia 2
OMIM ID 617137
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 MAP3K7
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00434624 251869 - - M ? ? (unknown) - - - - - FMD2 Neurodevelopmental abnormality, Delayed speech and language development, Hypotonia, Joint hypermobility, Aganglionic megacolon, Synophrys, Hypertrichosis, Cryptorchidism, Umbilical hernia, Patent foramen ovale, Supravalvular aortic stenosis MAP3K7 MAP3K7 1 1 Andreas Laner
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