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About:
Congenital cleft larynx and Opitz-Frias syndrome
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New Facet based on Instances of this Class
Attributes
Values
label
congenital cleft larynx and opitz-frias syndrome
COEXISTS_WITH
DELETION
ASSOCIATED_WITH
Mutation
schema:identifier
c0175696
ISA
Disease
Symptoms
Hereditary Diseases
Congenital Abnormality
Congenital Disorders
Hypospadias
PART_OF
C0030705
PROCESS_OF
C0030705
Family
Child
AFFECTS
C0030705
MANIFESTATION_OF
Disease
is
LOCATION_OF
of
Nose
Blood - brain barrier anatomy
22q11.2
Xp22
is
COEXISTS_WITH
of
Congenital Abnormality
Craniofacial Abnormalities
Eye Abnormalities
abnormal increase in the distance between two organs or parts
is
ASSOCIATED_WITH
of
ubiquitin-protein ligase
MID1|MPG
MID1 gene|MID1|MPG
is
DIAGNOSES
of
Magnetic Resonance Imaging
Chromosomal analysis
Dermatoglyphics
is
CAUSES
of
Genes
Mutation
Functional disorder
DELETION
MID1 gene|MID1|MPG
is
AFFECTS
of
IGBP1
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