Category:Genetic Disorders
From WikiMD's 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 415 total.
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- AADC deficiency
- Ackerman syndrome
- Acrogeria
- Adenoma sebaceum
- Adenosine deaminase 2 deficiency
- Akesson syndrome
- Albinism
- Albinism, yellow mutant type
- Alipogene tiparvovec
- Alpha thalassemia trait
- Amylo-1,6-glucosidase deficiency
- Andersen syndrome
- Andre syndrome
- Aniridia renal agenesis psychomotor retardation
- Anophthalmia Waardenburg syndrome
- Apert
- Apert syndrome
- Arachnodactyly
- Athabaskan brainstem dysgenesis syndrome
- Avellino corneal dystrophy
B
- Bainbridge-Ropers syndrome
- Bare lymphocyte syndrome type II
- Beck–Fahrner syndrome
- Beradinelli-Seip syndrome
- Berdon syndrome
- Beutler test
- Birt–Hogg–Dubé syndrome
- Bohring–Opitz syndrome
- Bone development disorder
- Brachydactyly anonychia
- Brachydactyly Mononen type
- Brachydactyly small stature face anomalies
- Breast cancer, familial
- Brittle bone syndrome lethal type
- Butyrate esterase
C
- CADASIL syndrome
- Calvarial hyperostosis
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Carnitine uptake defect
- Cataract anterior polar dominant
- Cataract dental syndrome
- Caudal regression syndrome
- CCA syndrome
- CCM syndrome
- CE
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- Cerebrofaciothoracic dysplasia
- Channelopathy
- Chemke–Oliver–Mallek syndrome
- 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
- Collagen, type VII, alpha 1
- Coloboma hair abnormality
- Color deficiency
- Combarros Calleja Leno syndrome
- Congenital alopecia X linked
- 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
- Contractural arachnodactyly
- Contractures ectodermal dysplasia cleft lip palate
- Coproporphyria
- Cormier–Rustin–Munnich syndrome
- Costeff optic atrophy syndrome
- Coxoauricular syndrome
- Cramer–Niederdellmann syndrome
- Craniofrontonasal syndrome Teebi type
- Craniosynostosis arthrogryposis cleft palate
- Craniosynostosis mental retardation heart defects
- Crawfurd syndrome
- Crouzonodermoskeletal syndrome
- Curry–Hall syndrome
- Cystinoses
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, autosomal dominant nonsyndromic sensorineural
- Deafness, isolated, due to mitochondrial transmission
- Defective expression of HLA class 2
- Dental aberrations steroid dehydrogenase deficienciency
- Dentin dysplasia
- Desmons syndrome
- Developmental delay epilepsy neonatal diabetes
- Diabetes hypogonadism deafness mental retardation
- Diaphragmatic defect limb deficiency skull defect
- Diaphragmatic hernia abnormal face limb
- Dienoyl-CoA reductase deficiency
- Dilated cardiomyopathy with ataxia syndrome
- Diprosopus
- Dismutase
- Distal arthrogryposis Moore–Weaver type
- Distal myopathy
- Distal myopathy Markesbery–Griggs type
- Dominant cleft palate
- Duncan
- Dwarfism bluish sclerae
- Dwarfism tall vertebrae
- Dwarfism thin bones multiple fractures
- Dysostosis peripheral
- Dystrophy
E
- Ectodermal dysplasia arthrogryposis diabetes mellitus
- 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-skin fragility syndrome
- Ectopic ossification familial type
- Ectrodactyly cleft palate syndrome
- Ectrodactyly-polydactyly syndrome
- Elliptocyte
- Emery-Dreifuss syndrome
- Enzyme deficiency
- Epidermolysis bullosa herpetiformis, Dowling–Meara
- Epidermolysis bullosa, junctional, Herlitz–Pearson
- Epidermolysis bullosa, pretibial
- Epidermolytic palmoplantar keratoderma Vorner type
- Epilepsy, partial, familial
- Epiphyseal dysplasia dysmorphism camptodactyly
- Erythrocyte fragility
- Escher Hirt syndrome
- Extrasystoles short stature hyperpigmentation microcephaly
- Exudative retinopathy, familial
F
- Factor xi deficiency
- Familial advanced sleep phase syndrome
- Familial ALS with dementia
- Feigenbaum Bergeron syndrome
- 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
G
- Gaucher-like disease
- Generalized trichoepithelioma
- Genital dwarfism, Turner type
- Ghent
- Giedion syndrome
- Glycogen debrancher deficiency
- GNE myopathy
- Goltz-Gorlin syndrome
- Gorlin Syndrome
- Growth deficiency brachydactyly unusual facies
- Growth mental deficiency syndrome of Myhre
- Growth retardation alopecia pseudoanodontia optic
H
- Halal Setton Wang syndrome
- Hand and foot deformity flat facies
- Harlequin
- Harris platelet syndrome
- Hay–Wells syndrome recessive type
- Heart defect round face congenital retarded development
- Heckenlively syndrome
- Heide syndrome
- Hemolytic
- Hemophiliac
- Heparane sulfamidase deficiency
- Hereditary breast–ovarian cancer syndrome
- Hereditary Multiple Exostoses
- Hereditary resistance to anti-vitamin K
- Hereditary sensory neuropathy type I
- Hereditary stomatocytosis
- Hereditary type 1 neuropathy
- High anterior hairline
- History of Tay–Sachs disease
- Holmes Collins syndrome
- Holmes–Collins syndrome
- Holoprosencephaly radial heart renal anomalies
- Homologous wasting disease
- Hypergonadotropic ovarian failure, familial or sporadic
- Hyperimmunoglobulin E syndrome
- Hyperplasia of midface
- Hyperprolinemia
- Hypertelorism
- Hypertrichosis congenital generalized X linked
- Hypohidrotic ectodermal dysplasia with immune deficiency
- Hypokalemic periodic paralysis
- Hypoparathyroidism familial isolated
- Hypoparathyroidism short stature mental retardation
