Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Preferred Name

RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 3

Synonyms

ALKYLDIHYDROXYACETONEPHOSPHATE SYNTHASE DEFICIENCY

ID

http://purl.bioontology.org/ontology/OMIM/600121

altLabel

ALKYLDIHYDROXYACETONEPHOSPHATE SYNTHASE DEFICIENCY

ALKYLGLYCERONE-PHOSPHATE SYNTHASE DEFICIENCY

AGPS DEFICIENCY

RCDP3

cui

C1838612

Gene Locus

2q31

Gene Symbol

AGPS

ADHAPS

RCDP3

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU000041

http://purl.bioontology.org/ontology/OMIM/MTHU006623

http://purl.bioontology.org/ontology/OMIM/MTHU000081

http://purl.bioontology.org/ontology/OMIM/MTHU006619

http://purl.bioontology.org/ontology/OMIM/MTHU006617

http://purl.bioontology.org/ontology/OMIM/MTHU006620

http://purl.bioontology.org/ontology/OMIM/MTHU029045

http://purl.bioontology.org/ontology/OMIM/MTHU006622

http://purl.bioontology.org/ontology/OMIM/MTHU006618

http://purl.bioontology.org/ontology/OMIM/MTHU006621

MIMTYPEMEANING

Phenotype description, molecular basis known.

notation

600121

OMIM Entry Type

3

OMIM MimType Value

pound

prefLabel

RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 3

tui

T047

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_0110853 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/MESH/C537608 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C537608 Medical Subject Headings LOOM