Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Chondrodysplasia Punctata, Rhizomelic

Synonyms

Rhizomelic Chondrodysplasia Punctata

Definitions

An autosomal recessive form of CHONDRODYSPLASIA PUNCTATA characterized by defective plasmalogen biosynthesis and impaired peroxisomes. Patients have shortened proximal limbs and severely disturbed endochondral bone formation. The metabolic defects associated with the impaired peroxisomes are present only in the rhizomelic form of chondrodysplasia punctata. (From Scriver et al, Metabolic Basis of Inherited Disease, 6th ed, p1497)

ID

http://purl.bioontology.org/ontology/MESH/D018902

altLabel

Rhizomelic Chondrodysplasia Punctata

Punctata, Rhizomelic Chondrodysplasia

Chondrodysplasia Punctata, Rhizomelic Form

Rhizomelic Chondrodysplasia Punctatas

Punctatas, Rhizomelic Chondrodysplasia

Chondrodysplasia Punctatas, Rhizomelic

AN

a form of osteochondrodysplasia with stippled epiphyses; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES

AQL

BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C0282529

DC

1

definition

An autosomal recessive form of CHONDRODYSPLASIA PUNCTATA characterized by defective plasmalogen biosynthesis and impaired peroxisomes. Patients have shortened proximal limbs and severely disturbed endochondral bone formation. The metabolic defects associated with the impaired peroxisomes are present only in the rhizomelic form of chondrodysplasia punctata. (From Scriver et al, Metabolic Basis of Inherited Disease, 6th ed, p1497)

DX

19960101

HN

1996

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469

Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D000326

http://purl.bioontology.org/ontology/MESH/D054078

http://purl.bioontology.org/ontology/MESH/D052919

http://purl.bioontology.org/ontology/MESH/D015211

http://purl.bioontology.org/ontology/MESH/D020642

http://purl.bioontology.org/ontology/MESH/D012035

Machine permutation

1996

Mapped from

http://purl.bioontology.org/ontology/MESH/C537607

http://purl.bioontology.org/ontology/MESH/C531651

http://purl.bioontology.org/ontology/MESH/C537608

MDA

19941227

MMR

20150608

MN

C05.116.099.708.195.200

C18.452.648.663.265

C16.320.565.663.265

notation

D018902

prefLabel

Chondrodysplasia Punctata, Rhizomelic

TERMUI

T751461

T056337

T056336

TH

NLM (1996)

NLM (2010)

ORD (2010)

OMIM (2013)

GHR (2014)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D002806

http://purl.bioontology.org/ontology/MESH/D018901

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/215100 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/ICD10CM/E71.540 International Classification of Diseases, Version 10 - Clinical Modification CUI