Source: HPO

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease
disease 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
phenotype 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0267048
Disease: Glossoptosis
Glossoptosis
disease 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0456070
Disease: Growth delay
Growth delay
phenotype 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects
group 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis
disease 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0020546
Disease: Hypertensive crisis
Hypertensive crisis
phenotype 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem
phenotype 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0452168
Disease: Hypospadias, balanic
Hypospadias, balanic
disease 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C1846462
Disease: Impaired ocular abduction
Impaired ocular abduction
phenotype 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
group 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0023075
Disease: Laryngostenosis
Laryngostenosis
disease 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C1865014
Disease: Long philtrum
Long philtrum
phenotype 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0221355
Disease: Macrocephaly
Macrocephaly
disease 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0025958
Disease: Microcephaly
Microcephaly
disease 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0025988
Disease: Microglossia
Microglossia
disease 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0025990
Disease: Micrognathism
Micrognathism
disease 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C1854301
Disease: Motor delay
Motor delay
phenotype 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
phenotype 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0026848
Disease: Myopathy
Myopathy
group 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0028866
Disease: Oculomotor Nerve Paralysis
Oculomotor Nerve Paralysis
disease 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
phenotype 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C1846477
Disease: Pectoralis hypoplasia
Pectoralis hypoplasia
phenotype 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0031900
Disease: Pierre Robin Syndrome
Pierre Robin Syndrome
disease 0.100 None 0 0
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
myomaker, myoblast fusion factor 0.659 0.538 1.8E-04
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly
disease 0.100 None 0 0