Disease #01710 (GRBGD (Greenberg skeletal dysplasia), OMIM:215140)

Official abbreviation GRBGD
Name Greenberg skeletal dysplasia
OMIM ID 215140
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene LBR
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

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00434444 256215 - prenatal trio exom after ultrasound abnormalities ? likely - - - - - - GRBGD Abnormality of prenatal development or birth, Skeletal dysplasia, Thickened nuchal skin fold, Micromelia, Postaxial polydactyly, Abnormal thorax morphology, Single umbilical artery LBR LBR 1 1 Andreas Laner
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