Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Neutropenia, Severe Congenital, X-Linked

ID

http://purl.bioontology.org/ontology/MESH/C564539

cui

C1845987

Has mapping qualifier

http://purl.bioontology.org/ontology/MESH/Q000151

HM

D040181

D009503/Q000151

Inverse of RB

0

Mapped to

http://purl.bioontology.org/ontology/MESH/D040181

http://purl.bioontology.org/ontology/MESH/D009503

MDA

20121105

MeSH Frequency

2

MMR

20131106

notation

C564539

prefLabel

Neutropenia, Severe Congenital, X-Linked

SC

3

TERMUI

T805088

TH

OMIM (2013)

tui

T047

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/300299 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/300299 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/OMIM/300392 Online Mendelian Inheritance in Man CUI