Source: HPO

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0345392
Disease: Congenital kyphoscoliosis
Congenital kyphoscoliosis 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0575158
Disease: Kyphoscoliosis deformity of spine
Kyphoscoliosis deformity of spine 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0595939
Disease: Stillbirth
Stillbirth 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0600033
Disease: Acquired Kyphoscoliosis
Acquired Kyphoscoliosis 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0700201
Disease: Dyssomnias
Dyssomnias 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0851578
Disease: Sleep Disorders
Sleep Disorders 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0853087
Disease: Nail abnormality
Nail abnormality 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0870082
Disease: Hyperkeratosis
Hyperkeratosis 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C0973461
Disease: Dysphasia
Dysphasia 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C1184923
Disease: Lumbar hyperlordosis
Lumbar hyperlordosis 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C1836047
Disease: Long face
Long face 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C1837463
Disease: Narrow face
Narrow face 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C1839546
Disease: Microretrognathia
Microretrognathia 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C1840006
Disease: Mild intrauterine growth retardation
Mild intrauterine growth retardation 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		0.100 Biomarker HPO

Entrez Id: 50814
Gene Symbol: NSDHL
NSDHL
CUI: C1850573
Disease: Slender build
Slender build 		0.100 Biomarker HPO