| Diseases | Rating | Bibliogr. | Expand |
---|
1 | Genetic Predisposition to Disease | 100 | + + | |
2 | Syndrome | 67 | + + | |
3 | Muscular Dystrophies | 4 | + + | |
4 | Intellectual Disability | 4 | + + | |
5 | Spastic Paraplegia, Hereditary | 3 | + + | |
6 | Mental Retardation, X-Linked | 2 | + + | |
7 | Eye Diseases, Hereditary | 2 | + + | |
8 | Cerebellar Ataxia | 2 | + + | |
9 | Charcot-Marie-Tooth Disease | 2 | + + | |
10 | Retinitis Pigmentosa | 2 | + + | |
11 | Muscular Dystrophy, Emery-Dreifuss | 2 | + + | |
12 | Dystonia Musculorum Deformans | 2 | + + | |
13 | Athetosis | 2 | + + | |
14 | Disease Susceptibility | 2 | + + | |
15 | Muscular Atrophy, Spinal | 2 | + + | |
16 | Cataract | 2 | + + | |
17 | Color Vision Defects | 2 | + + | |
18 | Albinism, Ocular | 2 | + + | |
19 | Chromosome Disorders | 2 | + + | |
20 | Abnormalities, Multiple | 2 | + + | |
21 | Thinness | 1 | + + | |
22 | Nephritis, Hereditary | 1 | + + | |
23 | Seizures, Febrile | 1 | + + | |
24 | Nystagmus, Congenital | 1 | + + | |
25 | Polycystic Kidney, Autosomal Dominant | 1 | + + | |
26 | Genetic Diseases, X-Linked | 1 | + + | |
27 | Migraine with Aura | 1 | + + | |
28 | Hereditary Sensory and Motor Neuropathy | 1 | + + | |
29 | Muscle Hypertonia | 1 | + + | |
30 | Chromosome Aberrations | 1 | + + | |
31 | Bipolar Disorder | 1 | + + | |
32 | Hyperkeratosis, Epidermolytic | 1 | + + | |
33 | Diabetes Mellitus, Type 2 | 1 | + + | |
34 | Auditory Diseases, Central | 1 | + + | |
35 | Dystonia | 1 | + + | |
36 | Hereditary Central Nervous System Demyelinating Diseases | 1 | + + | |
37 | Epispadias | 1 | + + | |
38 | Deafness | 1 | + + | |
39 | Osteochondrodysplasias | 1 | + + | |
40 | Spinocerebellar Degenerations | 1 | + + | |
41 | Myotonic Dystrophy | 1 | + + | |
42 | Autistic Disorder | 1 | + + | |
43 | Spinocerebellar Ataxias | 1 | + + | |
44 | Dysplastic Nevus Syndrome | 1 | + + | |
45 | Huntington Disease | 1 | + + | |
46 | Olfaction Disorders | 1 | + + | |
47 | Chorea | 1 | + + | |
48 | Muscular Dystrophies, Limb-Girdle | 1 | + + | |
49 | Muscle Rigidity | 1 | + + | |
50 | Dystonic Disorders | 1 | + + | |
51 | Microcephaly | 1 | + + | |
52 | Albinism | 1 | + + | |
53 | Muscular Atrophy | 1 | + + | |
54 | Tooth Diseases | 1 | + + | |
55 | Chromosome Deletion | 1 | + + | |
56 | Paraplegia | 1 | + + | |
57 | Fragile X Syndrome | 1 | + + | |
58 | Schizophrenia | 1 | + + | |
59 | Sex Chromosome Aberrations | 1 | + + | |
60 | Microphthalmos | 1 | + + | |
61 | Muscular Diseases | 1 | + + | |
62 | Pigmentation Disorders | 1 | + + | |
63 | Genetic Diseases, Inborn | 1 | + + | |
64 | Ataxia | 1 | + + | |
65 | Diffuse Cerebral Sclerosis of Schilder | 1 | + + | |
66 | Diseases in Twins | 1 | + + | |
67 | Hypotrichosis | 1 | + + | |
68 | Hypohidrosis | 1 | + + | |
69 | Hypolipoproteinemias | 1 | + + | |
70 | Epilepsy, Tonic-Clonic | 1 | + + | |
71 | Epilepsies, Myoclonic | 1 | + + | |
72 | Ectodermal Dysplasia | 1 | + + | |
73 | Muscle Spasticity | 1 | + + | |
74 | Branchio-Oto-Renal Syndrome | 1 | + + | |
75 | Nervous System Malformations | 1 | + + | |
76 | Parkinsonian Disorders | 1 | + + | |
77 | Chromosome Fragility | 1 | + + | |
78 | Hypogonadism | 1 | + + | |
79 | Adenomatous Polyposis Coli | 1 | + + | |
80 | Craniofacial Abnormalities | 1 | + + | |
81 | Fetal Diseases | 1 | + + | |
82 | Myositis, Inclusion Body | 1 | + + | |
83 | Tangier Disease | 1 | + + | |
84 | Marfan Syndrome | 1 | + + | |