Select item 442777 Glioma susceptibility 3 Select item 374932 Autoimmune thyroid disease, susceptibility to, 3 Autoimmune thyroid disease 3 Select item 9841 Azorean disease Azorean neurologic disease Machado-Joseph disease Nigrospinodentatal degeneration SPINOCEREBELLAR ATROPHY III Spinocerebellar Ataxia Type 3 Spinocerebellar atrophy type 3 Spinopontine atrophy Select item 462009 Breast-ovarian cancer, familial, susceptibility to, 3 Breast-ovarian cancer, familial 3 RAD51C-Related Breast/Ovarian Cancer RAD51C-Related Familial Susceptibility to Breast-Ovarian Cancer Select item 394222 SKIN/HAIR/EYE PIGMENTATION 3, LIGHT/DARK SKIN EYE COLOR 1 EYE COLOR, GREEN/BLUE SKIN/HAIR/EYE PIGMENTATION 3, BLUE/GREEN EYE COLOR SKIN/HAIR/EYE PIGMENTATION 3, FRECKLING Skin/hair/eye pigmentation, variation in, 3 Select item 78653 Gaucher disease type III GD 3 GD III Gaucher Disease Type 3 (Subacute/Chronic) Gaucher Disease, Type 3 Gaucher disease, chronic neuronopathic type Gaucher disease, juvenile and adult, cerebral Gaucher disease, subacute neuronopathic type Subacute neuronopathic Gaucher's disease Select item 155549 Neuronal ceroid lipofuscinosis 3 CLN3 Disease CLN3-Related Neuronal Ceroid-Lipofuscinosis Spielmeyer Sjogren disease Select item 461518 Smoking as a quantitative trait locus 3 Select item 414542 Atypical hemolytic-uremic syndrome with I factor anomaly AHUS, SUSCEPTIBILITY TO, 3 Atypical hemolytic-uremic syndrome 3 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3 Select item 373202 Melanoma, cutaneous malignant, susceptibility to, 3 CDK4-Related Cutaneous Malignant Melanoma Cutaneous malignant melanoma 3 Select item 199598 UDPglucose-4-epimerase deficiency Epimerase Deficiency Galactosemia GALACTOSEMIA III Galactose epimerase deficiency Galactosemia 3 UDP-Galactose-4-epimerase deficiency UDPglucose 4-Epimerase Deficiency Disease Select item 41678 Familial dysautonomia FD HSAN 3 HSAN III HSN 3 Hereditary sensory and autonomic neuropathy 3 Hereditary sensory neuropathy type 3 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III Riley Day syndrome Select item 346809 Nephronophthisis 3 Adolescent nephronophthisis Select item 394534 Axenfeld-Rieger syndrome type 3 AXENFELD-RIEGER ANOMALY WITH CARDIAC DEFECTS AND/OR SENSORINEURAL HEARING LOSS Anterior chamber cleavage syndrome Axenfeld-rieger anomaly with or without cardiac defects and/or sensorineural hearing loss Rieger syndrome type 3 Select item 101816 Kugelberg-Welander disease Juvenile Spinal Muscular Atrophy Kugelberg-Welander syndrome Muscular atrophy, juvenile SMA 3 SMA III SPINAL MUSCULAR ATROPHY, TYPE III Spinal muscular atrophy type 3 Spinal muscular atrophy, mild childhood and adolescent form Select item 156006 Spinocerebellar ataxia 7 ADCA type 2 ADCA, TYPE II Autosomal dominant cerebellar ataxia type 2 Autosomal dominant cerebellar ataxia type II OLIVOPONTOCEREBELLAR ATROPHY III OPCA III Olivopontocerebellar atrophy 3 Select item 86948 Waardenburg syndrome type 3 Klein-Waardenberg's syndrome Klein-Waardenburg syndrome Waardenburg Syndrome Type III Waardenburg syndrome with upper limb anomalies White forelock (poliosis) syndrome with multiple congenital malformations Select item 373333 Scoliosis, isolated, susceptibility to, 3 Select item 266075 von Willebrand disease type 3 Type 3 VWD Type 3 Von Willebrand's disease V WD3 VON WILLEBRAND DISEASE, TYPE III Von Willebrand disease, recessive form Von Willebrand disease, severe form Select item 327125 Holoprosencephaly 3 
