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: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0556280
Disease: Gross motor impairment
Gross motor impairment 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0349588
Disease: Short stature
Short stature 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0349506
Disease: Photosensitivity of skin
Photosensitivity of skin 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0311277
Disease: Obesity, Abdominal
Obesity, Abdominal 		phenotype 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers 		disease 0.100 None 0 0
Entrez Id: 3653
Gene Symbol: IPW
IPW 		imprinted in Prader-Willi syndrome 0.682 0.423
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		phenotype 0.100 None 0 0