Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024
Preferred Name

Stiff skin syndrome
Synonyms
Definitions

Stiff skin syndrome is a rare, slowly progressive cutaneous disease characterized by rock-hard skin bound firmly to the underlying tissues (mainly on the shoulders, lower back, buttocks and thighs), mild hypertrichosis and hyperpigmentation overlying the affected areas of skin, as well as limited joint mobility (mainly of large joints) with flexion contractures. Cutaneous nodules, affecting mostly distal interphalangeal joints, as well as extracutaneous manifestations, including diffuse entrapment neuropathy, scoliosis, a tiptoe gait and a narrow thorax, may be associated. Restrictive pulmonary changes, muscle weakness, short stature and growth delay have also been reported. No vascular hyperreactivity, immunologic abnormalities nor visceral, muscular or bone involvement has been described.

ID

http://www.orpha.net/ORDO/Orphanet_2833

definition

Stiff skin syndrome is a rare, slowly progressive cutaneous disease characterized by rock-hard skin bound firmly to the underlying tissues (mainly on the shoulders, lower back, buttocks and thighs), mild hypertrichosis and hyperpigmentation overlying the affected areas of skin, as well as limited joint mobility (mainly of large joints) with flexion contractures. Cutaneous nodules, affecting mostly distal interphalangeal joints, as well as extracutaneous manifestations, including diffuse entrapment neuropathy, scoliosis, a tiptoe gait and a narrow thorax, may be associated. Restrictive pulmonary changes, muscle weakness, short stature and growth delay have also been reported. No vascular hyperreactivity, immunologic abnormalities nor visceral, muscular or bone involvement has been described.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=2833

has_age_of_onset

Childhood

Infancy

Neonatal

hasDbXref

UMLS:C1861456

MeSH:C566112

ICD-10:L98.8

ICD-11:EE6Y

MedDRA:10085085

OMIM:184900

OMIM:228020

label

Stiff skin syndrome

notation

ORPHA:2833

part_of

http://www.orpha.net/ORDO/Orphanet_79385

prefixIRI

ORDO:Orphanet_2833

prefLabel

Stiff skin syndrome

present_in

Worldwide AND has_point_prevalence_range : <1 / 1 000 000

Worldwide AND has_cases/families_value : 54.0 (Case)

treeView

http://www.orpha.net/ORDO/Orphanet_79385

subClassOf

http://www.orpha.net/ORDO/Orphanet_377788

http://www.orpha.net/ORDO/Orphanet_557493

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Delete Mapping To Ontology Source
http://www.orpha.net/ORDO/Orphanet_2833 CCONT SAME_URI
http://www.orpha.net/ORDO/Orphanet_2833 EFO SAME_URI
http://purl.bioontology.org/ontology/OMIM/184900 OMIM LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118636 NCIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C566112 RH-MESH LOOM
http://purl.obolibrary.org/obo/OMIM_184900 CCO LOOM
http://www.owl-ontologies.com/unnamed.owl#RID14742 DERMLEX LOOM
rgo:29399 GAMUTS LOOM
http://purl.bioontology.org/ontology/MEDDRA/10085085 MEDDRA LOOM
http://www.limics.org/hrdo/rdfns#pat_id_2570 HRDO LOOM
http://purl.obolibrary.org/obo/MONDO_0008492 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0008492 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0008492 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0008492 DOVES LOOM
http://purl.obolibrary.org/obo/DERMO_0001910 DERMO LOOM
http://purl.bioontology.org/ontology/MESH/C566112 MESH LOOM
http://identifiers.org/omim/184900 REXO LOOM
http://identifiers.org/omim/184900 GEXO LOOM
http://identifiers.org/omim/184900 RETO LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/765187004 SNOMEDCT LOOM
http://purl.obolibrary.org/obo/NCIT_C118636 BERO LOOM
http://purl.obolibrary.org/obo/DOID_0111561 DOID LOOM
http://purl.obolibrary.org/obo/DOID_0111561 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_0111561 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_0111561 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0111561 FNS-H LOOM
http://www.gamuts.net/entity#stiff_skin_syndrome GAMUTS REST