Disease #02890 (GLND (glutamine deficiency, congenital), OMIM:610015)

Official abbreviation GLND
Name glutamine deficiency, congenital
OMIM ID 610015
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GLUL
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-09-05 19:37:35 +02:00 (CEST)


Individuals

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00472252 - Verebi et al. (submitted) - M - France - - - - - GLND 0005684: Distal arthrogryposis, 0000954: Single transverse palmar crease - GLDN, GLUL 2 1 Camille Verebi
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