Disease #00171 (SNDNS (SNEDDON SYNDROME), OMIM:182410)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	SNDNS
Name	SNEDDON SYNDROME
OMIM ID	182410
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ADA2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-28 12:48:54 +00:00 (UTC)
Date last edited	N/A