| 2885 |
Ciliary dyskinesia, primary, DNAI1-related |
1 |
Human disease
|
5.0 |
| 2886 |
Long QT syndrome, CACNA1C-related |
1 |
Human disease
|
5.0 |
| 2887 |
Ectodermal dysplasia, EDARADD-related |
3 |
Human disease
|
5.0 |
| 2891 |
Lissencephaly, DCX-related |
1 |
Human disease
|
10.0 |
| 2892 |
Microcephaly, ASPM-related |
1 |
Human disease
|
5.0 |
| 2894 |
Woodhouse-Sakati syndrome |
1 |
Human disease
|
5.0 |
| 2895 |
Haplotype with homozygous deficiency, SEL05, SEL07, SEL18 |
1 |
Animal disease only
|
|
| 2902 |
Osteochondrodysplastic and cardiomyopathic syndrome |
1 |
Human disease
|
9.0 |
| 2903 |
Visceral white-nodules disease, susceptibility/resistance to |
1 |
Animal disease only
|
|
| 2904 |
Male subfertility, EML5-related |
1 |
Animal disease only
|
|
| 2905 |
Polyglucosan storage disease, generic |
1 |
Animal disease only
|
|
| 2906 |
Pontocerebellar hypoplasia, generic |
1 |
Animal disease only
|
|
| 2909 |
Ataxia, episodic |
1 |
Human disease
|
6.5 |
| 2910 |
Sjogren syndrome |
2 |
Human disease
|
42.0 |
| 2911 |
Peracute mortality syndrome |
1 |
Animal disease only
|
|
| 2912 |
Ciliopathy, CPLANE1-related |
1 |
Target evidence
|
56.3 |
| 2913 |
Cardiac malformation, BRI3BP-related |
1 |
Animal disease only
|
|
| 2914 |
Cystic eye, congenital |
1 |
Human disease
|
6.5 |
| 2915 |
Apolipoprotein C-II deficiency |
1 |
Animal disease only
|
|
| 2916 |
Charcot-Marie-Tooth disease, ITPR3-related |
1 |
Target evidence
|
57.0 |
| 2917 |
Hyperbiliverdinaemia |
1 |
Target evidence
|
55.6 |
| 2918 |
Myopathy, 'dozer lamb syndrome' |
1 |
Animal disease only
|
|
| 2919 |
Carcinoma, gastric, predisposition to |
1 |
Animal disease only
|
|
| 2920 |
Precocious puberty, MKRN3-related |
1 |
Human disease
|
10.0 |
| 2922 |
Ataxia with isolated vitamin E deficiency |
1 |
Target evidence
|
62.8 |
| 2923 |
Posthitis, predisposition to |
1 |
Animal disease only
|
|
| 2924 |
Anhidrosis, generic |
1 |
Human disease
|
9.0 |
| 2926 |
Retinal atrophy, progressive, GTPBP2-related |
1 |
Target evidence
|
56.0 |
| 2929 |
Nephronophthisis |
2 |
Human disease
|
12.0 |
| 2932 |
Stomatocytosis |
1 |
Animal disease only
|
|
| 2933 |
Aortic valve stenosis, generic |
1 |
Human disease
|
9.0 |
| 2934 |
Toxoplasma gondii infection, susceptibility/resistance to |
2 |
Animal disease only
|
|
| 2938 |
Scuticociliatosis, susceptibility/resistance to |
1 |
Animal disease only
|
|
| 2939 |
Epileptic encephalopathy, CAD-related |
1 |
Target evidence
|
57.1 |
| 2940 |
Cataract, CPT1A-related |
1 |
Animal disease only
|
|
| 2941 |
Duck hepatitis A virus, susceptibility/resistance to |
1 |
Animal disease only
|
|
| 2942 |
Fish allergen, parvalbumin |
1 |
Animal disease only
|
|
| 2943 |
Retinal atrophy, progressive, JPH2-related |
1 |
Animal disease only
|
|
| 2944 |
Patched1-deficiency |
1 |
Animal disease only
|
|
| 2945 |
Hypogonadism, RLN3B-related |
1 |
Animal disease only
|
|
| 2947 |
Skeletal abnormality, BMP6-related |
1 |
Animal disease only
|
|
| 2948 |
Adrenal hyperplasia, congenital, CYP21A2-related |
1 |
Human disease
|
30.0 |
| 2949 |
Gamatogenic failure, TERB1-related |
1 |
Human disease
|
5.0 |
| 2950 |
Mitochondrial DNA depletion syndrome, MPV17-related |
1 |
Human disease
|
5.0 |
| 2951 |
Cardiomyopathy, hypertrophic, MYBPC3-related, autosomal dominant |
1 |
Target evidence
|
58.5 |
| 2952 |
Cardiomyopathy, hypertrophic, MYBPC3-related, autosomal recessive |
1 |
Target evidence
|
58.5 |
| 2953 |
Cardiomyopathy, hypertrophic, MYH6-related |
1 |
Human disease
|
5.0 |
| 2954 |
Neutrophilic dermatosis |
1 |
Human disease
|
9.0 |
| 2955 |
Adrenoleukodystrophy, ABCD1-related |
1 |
Human disease
|
30.0 |
| 2957 |
Anophthalmia/microphthalmia, GJA8-related |
1 |
Human gene
|
21.0 |
