Disease #05193 (SEMDFA (dysplasia, spondylopeimetaphyseal, Faden-Alkuraya type (SEMDFA)), OMIM:616723)

Official abbreviation SEMDFA
Name dysplasia, spondylopeimetaphyseal, Faden-Alkuraya type (SEMDFA)
OMIM ID 616723
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 RSPRY1
Associated tissues -
Disease features -
Remarks -
Date created 2016-10-11 10:19:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00065293 26365341-Fam2PatII1 PubMed: Faden 2015, Journal: Faden 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Canada Peruvian >07y06m - - - SEMDFA diagnosed as Progressive Skeletal Dysplasia; short stature (HP:0004322), Intellectual disability (HP:0001249), Motor delay (HP:0001270), Delayed skeletal maturation (HP:0002750), Microcephaly (HP:0000252), Abnormal facial shape (HP:0001999), Overlapping toe (HP:0001845), Scoliosis (HP:0002650), no craniosynostosis (-HP:0001363), Carpal bone hypoplasia (HP:0001498), Platyspondyly (HP:0000926), Short femoral neck (HP:0100864), Short fourth metatarsal (HP:0004689), Cupped metaphyses of hand bones (HP:0004273) RSPRY1 RSPRY1 1 1 Pieter Klap
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