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
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
Displaying 1 entry
Gene ID Gene Symbol Description Source
40281 Pss Phosphatidylserine synthase
The Human Phenotype Ontology
Displaying entries 51 - 60 of 102 in total
HPO ID HPO Term
HP:0007495 Prematurely aged appearance
HP:0008065 Aplasia/Hypoplasia of the skin
HP:0009773 Symphalangism affecting the phalanges of the hand
HP:0010628 Facial palsy
HP:0011001 Increased bone mineral density
HP:0011002 Osteopetrosis
HP:0012471 Thick vermilion border
HP:0100541 Femoral hernia
HP:0000006 Autosomal dominant inheritance
HP:0000041 Chordee
Displaying 1 entry
Gene ID Gene Symbol Description
9791 PTDSS1 phosphatidylserine synthase 1

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024