Category:Genetic Disorders
From WikiMD's Food, Medicine & Wellness Encyclopedia
This is a category page. It lists all of the pages in category "Genetic Disorders" as well as all subcategories of category "Genetic Disorders" if any exist.
Pages in category "Genetic Disorders"
The following 200 pages are in this category, out of 524 total.
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- Ackerman syndrome
- Acrogeria
- Adenoma sebaceum
- Adenosine deaminase 2 deficiency
- Albinism
- Albright
- Alipogene tiparvovec
- Alpha thalassemia trait
- Andersen syndrome
- Aniridia renal agenesis psychomotor retardation
- Apert
- Apert syndrome
- Arachnodactyly
- Aspartylglucosylamine deaspartylase
- Athabaskan brainstem dysgenesis syndrome
B
- Bare lymphocyte syndrome type II
- Beck–Fahrner syndrome
- Benign familial infantile convulsions
- Benjamin Syndrome
- Berdon syndrome
- Beutler test
- Biliary atresia, intrahepatic, syndromic form
- Birth Defects Research
- Birt–Hogg–Dubé syndrome
- Blepharophimosis nasal groove growth retardation
- Bohring–Opitz syndrome
- Bone development disorder
- Bone fragility craniosynostosis proptosis hydrocephalus
- Bonnemann–Meinecke syndrome
- Brachman-de Lange syndrome
- Brachydactyly anonychia
- Brachydactyly Mononen type
- Brachydactyly small stature face anomalies
- Brittle bone syndrome lethal type
- Butyrate esterase
C
- C1-INH
- CADASIL syndrome
- Calvarial hyperostosis
- Camptodactyly joint contractures facial skeletal dysplasia
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Cataract anterior polar dominant
- Cataract dental syndrome
- Caudal regression syndrome
- CCA syndrome
- CE
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- Channelopathy
- Chemke–Oliver–Mallek syndrome
- Choanal atresia deafness cardiac defects dysmorphia
- Cholesterol and steroid metabolism disorders
- Chondrodysplasia punctata, Sheffield type
- Choroideremia hypopituitarism
- CHST14
- Ciliary discoordination, due to random ciliary orientation
- Ciliary dyskinesia-bronchiectasis
- CLCN1
- Cleft lip palate ectrodactyly
- Cleft lip palate mental retardation corneal opacity
- Cleft lip palate oligodontia syndactyly pili torti
- Cleft lip palate-tetraphocomelia
- Cleft lower lip cleft lateral canthi chorioretinal
- COL6A1
- COL9A1
- Cole–Carpenter syndrome
- Coloboma hair abnormality
- Color deficiency
- Congenital alopecia X linked
- Congenital diseases
- Congenital estrogen deficiency
- Congenital heart disease radio ulnar synostosis mental retardation
- Congenital hemolytic anemia
- Congenital hyperinsulinism
- Congenital hypoplastic anemia
- Congenital muscular dystrophy
- Congenital myopathy
- Congenital short bowel
- Continuous muscle fiber activity hereditary
- Contractural arachnodactyly
- Contractures ectodermal dysplasia cleft lip palate
- Cormier–Rustin–Munnich syndrome
- Corneal anesthesia deafness mental retardation
- Coxoauricular syndrome
- Cramer–Niederdellmann syndrome
- Craniofrontonasal syndrome Teebi type
- Craniometaphyseal dysplasia dominant type
- Craniosynostosis arthrogryposis cleft palate
- Craniosynostosis mental retardation heart defects
- Craniosynostosis synostoses hypertensive nephropathy
- Crawfurd syndrome
- Crouzonodermoskeletal syndrome
- Cryptorchidism arachnodactyly mental retardation
- Curry–Hall syndrome
D
- De novo mutation
- Deaf blind hypopigmentation
- Deafness conductive stapedial ear malformation facial palsy
- Deafness goiter stippled epiphyses
- Deafness hypospadias metacarpal and metatarsal syndrome
- Deafness onychodystrophy dominant form
- Deafness, autosomal dominant nonsyndromic sensorineural
- Deafness, isolated, due to mitochondrial transmission
- Defective expression of HLA class 2
- Deficiency of the interleukin-1 receptor antagonist (DIRA)
- Dental aberrations steroid dehydrogenase deficienciency
- Dentin dysplasia
- Developmental delay epilepsy neonatal diabetes
- Developmental delay hypotonia extremities hypertrophy
- Diabetes hypogonadism deafness mental retardation
- Diaphragmatic defect limb deficiency skull defect
- Diaphragmatic hernia abnormal face limb
- Dihydroorotase
- Dilated cardiomyopathy with ataxia syndrome
- Diprosopus
- Dismutase
- Distal arthrogryposis Moore–Weaver type
- Distal myopathy
- Distal myopathy Markesbery–Griggs type
- Disturbances of human pigmentation
- Disturbances of pigmentation
- DSDs
- Duncan
- Dwarfism bluish sclerae
- Dwarfism mental retardation eye abnormality
- Dwarfism short limb absent fibulas very short digits
- Dwarfism stiff joint ocular abnormalities
- Dwarfism tall vertebrae
- Dwarfism thin bones multiple fractures
- Dysmorphism abnormal vocalization mental retardation
- Dysostosis peripheral
- Dystrophy
E
- Ectodermal dysplasia arthrogryposis diabetes mellitus
- Ectodermal dysplasia Bartalos type
- Ectodermal dysplasia blindness
- Ectodermal dysplasia hypohidrotic autosomal dominant
- Ectodermal dysplasia Margarita type
- Ectodermal dysplasia mental retardation syndactyly
- Ectodermal dysplasia neurosensory deafness
- Ectodermal dysplasia with corkscrew hairs
- Ectodermal dysplasia, hydrotic
- Ectodermal dysplasia, hypohidrotic, autosomal recessive
- Ectopic ossification familial type
- Ectrodactyly cleft palate syndrome
- Ectrodactyly-polydactyly syndrome
- Elliptocyte
- Emery-Dreifuss syndrome
- Enzyme deficiency
- Epidermolysis bullosa dystrophica, Bart type
- Epidermolysis bullosa herpetiformis, Dowling–Meara
- Epidermolysis bullosa simplex, Koebner type
- Epidermolysis bullosa, dermolytic
- Epidermolysis bullosa, junctional, Herlitz–Pearson
- Epidermolysis bullosa, pretibial
- Epidermolytic palmoplantar keratoderma Vorner type
- Epilepsy microcephaly skeletal dysplasia
- Epilepsy, partial, familial
- Epiphyseal dysplasia dysmorphism camptodactyly
- Erythrocyte fragility
- Erythrokeratodermia variabilis ichthyosis
- Extrasystoles short stature hyperpigmentation microcephaly
- Exudative retinopathy, familial
F
- Facies unusual arthrogryposis advanced skeletal malformations
- Factor VIII
- Factor xi deficiency
- Familial ALS with dementia
- Female pseudohermaphrodism Genuardi type
- Fetal akinesia syndrome X linked
- Fibular hypoplasia scapulo pelvic dysplasia absent
- Focal facial dermal dysplasia
- Follicular atrophoderma
- Fraser-like syndrome
- Frias syndrome
- Fryns–Fabry–Remans syndrome
G
- G6PDH
- Gaucher-like disease
- Generalized trichoepithelioma
- Genetics of autism
- Genital dwarfism, Turner type
- Genu valgum, st. Helena familial
- Ghent
- Giedion syndrome
- Gigantism partial, nevi, hemihypertrophy, macrocephaly
- Glaucoma ecopia microspherophakia stiff joints short stature
- Gonadal dysgenesis
- Goniodysgenesis mental retardation short stature
- Gorlin Syndrome
- Growth deficiency brachydactyly unusual facies
- Growth mental deficiency syndrome of Myhre
- Growth retardation alopecia pseudoanodontia optic
