Disease #06311 (MFRG (Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome), OMIM:618142)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	MFRG
Name	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome
OMIM ID	618142
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CTU2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.