Source: HPO

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0231679
Disease: Ulnar deviation of the fingers
Ulnar deviation of the fingers 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0041105
Disease: Trismus
Trismus 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0578038
Disease: Thin lips
Thin lips 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0426886
Disease: Tapering fingers (finding)
Tapering fingers (finding) 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C1854494
Disease: Slow progression
Slow progression 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0349588
Disease: Short stature
Short stature 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C1854114
Disease: Short nose
Short nose 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C3494422
Disease: Retrognathia
Retrognathia 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0033377
Disease: Ptosis
Ptosis 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0031900
Disease: Pierre Robin Syndrome
Pierre Robin Syndrome 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C1846477
Disease: Pectoralis hypoplasia
Pectoralis hypoplasia 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0028866
Disease: Oculomotor Nerve Paralysis
Oculomotor Nerve Paralysis 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0026848
Disease: Myopathy
Myopathy 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C1854301
Disease: Motor delay
Motor delay 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0025990
Disease: Micrognathism
Micrognathism 		0.100 Biomarker HPO

Entrez Id: 389827
Gene Symbol: MYMK
MYMK
CUI: C0025988
Disease: Microglossia
Microglossia 		0.100 Biomarker HPO