CDC/NIH Web Information Database
Last data update: May 20, 2024. (Total: 8777 Documents)
CDC/NIH Web Information |
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Macrothrombocytopenia progressive deafness
From NCATS Genetic and Rare Diseases Information Center |
Microcephaly deafness syndrome
From NCATS Genetic and Rare Diseases Information Center |
Enchondromatosis dwarfism deafness
From NCATS Genetic and Rare Diseases Information Center |
Deafness conductive ptosis skeletal anomalies
From NCATS Genetic and Rare Diseases Information Center |
Albinism deafness syndrome
From NCATS Genetic and Rare Diseases Information Center |
Albinism ocular late onset sensorineural deafness
From NCATS Genetic and Rare Diseases Information Center |
Arthritis short stature deafness
From NCATS Genetic and Rare Diseases Information Center |
Arthrogryposis-like hand anomaly and sensorineural deafness
From NCATS Genetic and Rare Diseases Information Center |
Cardiomyopathy diabetes deafness
From NCATS Genetic and Rare Diseases Information Center |
Cardiomyopathy and deafness due to tRNA lysine gene mutation
From NCATS Genetic and Rare Diseases Information Center |
Cataract ataxia deafness
From NCATS Genetic and Rare Diseases Information Center |
Caudal appendage deafness
From NCATS Genetic and Rare Diseases Information Center |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss
From NCATS Genetic and Rare Diseases Information Center |
Cleft palate colobomata radial synostosis deafness
From NCATS Genetic and Rare Diseases Information Center |
Conductive deafness with malformed external ear
From NCATS Genetic and Rare Diseases Information Center |
Corneal dystrophy and perceptive deafness
From NCATS Genetic and Rare Diseases Information Center |
Craniofacial deafness hand syndrome
From NCATS Genetic and Rare Diseases Information Center |
Deafness conductive stapedial ear malformation facial palsy
From NCATS Genetic and Rare Diseases Information Center |
Deafness craniofacial syndrome
From NCATS Genetic and Rare Diseases Information Center |
Deafness enamel hypoplasia nail defects
From NCATS Genetic and Rare Diseases Information Center |
Deafness, epiphyseal dysplasia, short stature
From NCATS Genetic and Rare Diseases Information Center |
Deafness goiter stippled epiphyses
From NCATS Genetic and Rare Diseases Information Center |
Deafness hyperuricemia neurologic ataxia
From NCATS Genetic and Rare Diseases Information Center |
Deafness hypogonadism syndrome
From NCATS Genetic and Rare Diseases Information Center |
Deafness hypospadias metacarpal and metatarsal syndrome
From NCATS Genetic and Rare Diseases Information Center |
Deafness mesenteric diverticula of small bowel neuropathy
From NCATS Genetic and Rare Diseases Information Center |
Deafness mixed with perilymphatic Gusher, X-linked
From NCATS Genetic and Rare Diseases Information Center |
Deafness nephritis anorectal malformation
From NCATS Genetic and Rare Diseases Information Center |
Deafness oligodontia syndrome
From NCATS Genetic and Rare Diseases Information Center |
Deafness peripheral neuropathy arterial disease
From NCATS Genetic and Rare Diseases Information Center |