Disease #06467 (NSLH2 (Noonan syndrome-like disorder with loose anagen hair 2), OMIM:617506)

Official abbreviation NSLH2
Name Noonan syndrome-like disorder with loose anagen hair 2
OMIM ID 617506
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PPP1CB
Associated tissues -
Disease features -
Remarks -

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