Human Disease Ontology

Last uploaded: November 27, 2024
Preferred Name

chondrodysplasia punctata
Synonyms

Chondrodysplasia punctata congenita

Definitions

A syndrome that is characterized by abnormal calcification of the epiphyses, causing stippling in radiography. DeObs MGI.

ID

http://purl.obolibrary.org/obo/DOID_2581

comment

DeObs MGI.

database_cross_reference

SNOMEDCT_US_2023_03_01:205486004

ICD10CM:Q77.3

UMLS_CUI:C0008445

MESH:D002806

GARD:8542

MIM:215105

NCI:C84632

ORDO:93442

definition

A syndrome that is characterized by abnormal calcification of the epiphyses, causing stippling in radiography.

disease has basis in

http://purl.obolibrary.org/obo/SO_0000704

has exact synonym

Chondrodysplasia punctata congenita

has narrower match

MESH:D002806

has_obo_namespace

disease_ontology

id

DOID:2581

in_subset

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

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

label

chondrodysplasia punctata

notation

DOID:2581

prefLabel

chondrodysplasia punctata

subClassOf

http://purl.obolibrary.org/obo/DOID_0050177

http://purl.obolibrary.org/obo/DOID_225

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_2581 CLO SAME_URI
http://purl.obolibrary.org/obo/DOID_2581 DTO SAME_URI
http://purl.obolibrary.org/obo/DOID_2581 BAO SAME_URI
http://purl.obolibrary.org/obo/DOID_2581 HHEAR SAME_URI
http://purl.obolibrary.org/obo/DOID_2581 DDSS SAME_URI
http://purl.obolibrary.org/obo/DOID_2581 NIFSTD SAME_URI
http://purl.obolibrary.org/obo/DOID_2581 FNS-H SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019701 MONDO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#2898 OCHV LOOM
http://www.owl-ontologies.com/unnamed.owl#RID15377 DERMLEX LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D002806 RH-MESH LOOM
http://www.limics.org/hrdo/rdfns#pat_id_12353 HRDO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10087150 MEDDRA LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Chondrodysplasia_Punctata CSEO LOOM
http://purl.bioontology.org/ontology/ICD10/Q77.3 ICD10 LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/278715001 SNOMEDCT LOOM
http://purl.jp/bio/4/id/200906065522493237 IOBC LOOM
http://purl.bioontology.org/ontology/MESH/D002806 MESH LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0008445 OCHV LOOM
http://www.phoc.org.cn/pmo/class/PMO_00036722 PMAPP-PMO LOOM
rgo:12498 GAMUTS LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84632 NCIT LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU050816 OMIM LOOM
http://purl.obolibrary.org/obo/DOID_2581 CLO LOOM
http://purl.obolibrary.org/obo/DOID_2581 DTO LOOM
http://purl.obolibrary.org/obo/DOID_2581 BAO LOOM
http://purl.obolibrary.org/obo/DOID_2581 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_2581 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_2581 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_2581 FNS-H LOOM
http://purl.bioontology.org/ontology/RCTV2/PG4C.00 RCTV2 LOOM
http://nanbyodata.jp/ontology/NANDO_2201017 NANDO LOOM
http://www.orpha.net/ORDO/Orphanet_93442 ORDO LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q77.3 ICD10CM LOOM
http://purl.obolibrary.org/obo/OMIT_0004126 OMIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C05.116.099.708.195 RH-MESH LOOM
http://purl.obolibrary.org/obo/MONDO_0019701 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0019701 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0019701 DOVES LOOM
http://purl.obolibrary.org/obo/NCIT_C84632 BERO LOOM
http://www.gamuts.net/entity#chondrodysplasia_punctata GAMUTS REST