Lenz-Majewski hyperostotic dwarfism

Summary
Synonym
  • Lenz-Majewski syndrome
Definition
A syndrome characterized by intellectual disability, sclerosing bone dysplasia, distinct craniofacial, dental, cutaneous and distal-limb anomalies that has_material_basis_in heterozygous mutation in the PTDSS1 gene on chromosome 8q22.1.
Super Class
autosomal dominant disease syndrome
External Links
Disease Ontology
DOID:0111507
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9791 PTDSS1 phosphatidylserine synthase 1
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P48651 Phosphatidylserine synthase 1
The Human Phenotype Ontology
Displaying entries 31 - 40 of 102 in total
HPO ID HPO Term
HP:0001376 Limitation of joint mobility
HP:0001382 Joint hypermobility
HP:0001582 Redundant skin
HP:0001804 Hypoplastic fingernail
HP:0001812 Hyperconvex fingernails
HP:0002650 Scoliosis
HP:0002684 Thickened calvaria
HP:0002705 High, narrow palate
HP:0002750 Delayed skeletal maturation
HP:0002808 Kyphosis
Displaying 1 entry
Gene ID Gene Symbol Description
9791 PTDSS1 phosphatidylserine synthase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024