Human Health Exposure Analysis Resource

Last uploaded: July 19, 2024
Preferred Name

occipital horn syndrome
Synonyms

Ehlers-Danlos syndrome type 9

Ehlers-Danlos syndrome type IX

EDS IX

X-linked cutis laxa

Definitions

A metal metabolism disorder characterized by hyperelastic and bruisable skin, hernias, bladder diverticula, hyperextensible joints, varicosities, abnormal copper transport, and multiple skeletal abnormalities that has_material_basis_in X-linked recessive inheritance of mutations in ATP7A on Xq21.1. This disorder is allelic to Menkes disease.

ID

http://purl.obolibrary.org/obo/DOID_0111272

alternative label

Ehlers-Danlos syndrome type 9

Ehlers-Danlos syndrome type IX

EDS IX

X-linked cutis laxa

database_cross_reference

UMLS_CUI:C0268353

MESH:C537860

SNOMEDCT_US_2023_03_01:59399004

GARD:4017

MIM:304150

ORDO:198

definition

A metal metabolism disorder characterized by hyperelastic and bruisable skin, hernias, bladder diverticula, hyperextensible joints, varicosities, abnormal copper transport, and multiple skeletal abnormalities that has_material_basis_in X-linked recessive inheritance of mutations in ATP7A on Xq21.1. This disorder is allelic to Menkes disease.

has exact synonym

Ehlers-Danlos syndrome type 9

Ehlers-Danlos syndrome type IX

EDS IX

X-linked cutis laxa

has material basis in

http://purl.obolibrary.org/obo/GENO_0000149

has_obo_namespace

disease_ontology

id

DOID:0111272

in_subset

http://purl.obolibrary.org/obo/doid#DO_rare_slim

label

occipital horn syndrome

notation

DOID:0111272

note

A metal metabolism disorder characterized by hyperelastic and bruisable skin, hernias, bladder diverticula, hyperextensible joints, varicosities, abnormal copper transport, and multiple skeletal abnormalities that has_material_basis_in X-linked recessive inheritance of mutations in ATP7A on Xq21.1. This disorder is allelic to Menkes disease.

preferred label

occipital horn syndrome

prefLabel

occipital horn syndrome

subClassOf

http://purl.obolibrary.org/obo/DOID_896

http://purl.obolibrary.org/obo/DOID_0080012

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_0111272 DOID SAME_URI
http://purl.obolibrary.org/obo/DOID_0111272 DOID SAME_URI
http://purl.obolibrary.org/obo/DOID_0111272 DDSS SAME_URI
http://purl.obolibrary.org/obo/DOID_0111272 NIFSTD SAME_URI
http://purl.obolibrary.org/obo/DOID_0111272 FNS-H SAME_URI
http://purl.obolibrary.org/obo/DOID_0111272 DOID LOOM
http://purl.obolibrary.org/obo/MONDO_0010572 MONDO LOOM
http://www.limics.org/hrdo/rdfns#pat_id_7035 HRDO LOOM
http://purl.obolibrary.org/obo/OMIM_304150 CCO LOOM
http://purl.obolibrary.org/obo/DOID_0111272 DOID LOOM
http://purl.obolibrary.org/obo/DOID_0111272 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_0111272 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0111272 FNS-H LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C537860 RH-MESH LOOM
rgo:10327 GAMUTS LOOM
http://www.orpha.net/ORDO/Orphanet_198 ORDO LOOM
http://purl.bioontology.org/ontology/MESH/C537860 MESH LOOM
http://purl.obolibrary.org/obo/DERMO_0001836 DERMO LOOM
http://purl.bioontology.org/ontology/OMIM/304150 OMIM LOOM
http://purl.bioontology.org/ontology/RCD/X40QP RCD LOOM
http://identifiers.org/omim/304150 REXO LOOM
http://identifiers.org/omim/304150 GEXO LOOM
http://identifiers.org/omim/304150 RETO LOOM
http://nanbyodata.jp/ontology/NANDO_2200581 NANDO LOOM
http://purl.obolibrary.org/obo/MONDO_0010572 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0010572 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0010572 DOVES LOOM
http://nanbyodata.jp/ontology/NANDO_1200654 NANDO LOOM