Disease #00107 (WTSN (WATSON SYNDROME), OMIM:193520)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	WTSN
Name	WATSON SYNDROME
OMIM ID	193520
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	INS, NF1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-16 09:48:05 +00:00 (UTC)
Date last edited	N/A