Category:Genetic syndromes
Appearance
Subcategories
This category has the following 2 subcategories, out of 2 total.
G
R
Pages in category "Genetic syndromes"
The following 164 pages are in this category, out of 164 total. This list may not reflect recent changes.
A
- Absence of fingerprints-congenital milia syndrome
- Absent tibia-polydactyly-arachnoid cyst syndrome
- ADNP syndrome
- Al Gazali Sabrinathan Nair syndrome
- Al-Gazali-Donnai-Mueller syndrome
- Al-Raqad syndrome
- Alazami syndrome
- Alwadei syndrome
- Andermann syndrome
- Apparent mineralocorticoid excess syndrome
- Arts syndrome
- ATR-X syndrome
- Autism with port-wine stain syndrome
B
- Bamforth–Lazarus syndrome
- Barakat-Perenthaler syndrome
- Biemond syndrome
- Birk-Barel syndrome
- Blepharoptosis-myopia-ectopia lentis syndrome
- Börjeson–Forssman–Lehmann syndrome
- Boucher-Neuhäuser syndrome
- Boudhina-Yedes-Khiari syndrome
- Brachydactyly-long thumb syndrome
- Brachydactyly-preaxial hallux varus syndrome
- Branchio-oculo-facial syndrome
- Bruck syndrome
- Brunner syndrome
C
- Camera–Marugo–Cohen syndrome
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Camptodactyly-taurinuria syndrome
- Camptodactyly, tall stature, and hearing loss syndrome
- Cardiospondylocarpofacial syndrome
- Carey Fineman Ziter syndrome
- Cataract-ataxia-deafness syndrome
- CHAMP1-associated intellectual disability syndrome
- CHARGE syndrome
- Chromosomal deletion syndrome
- Cole–Carpenter syndrome
- Collins–Pope syndrome
- Coloboma of macula-brachydactyly type B syndrome
- Contiguous gene syndrome
- Costeff syndrome
- Cousin syndrome
- Cousin–Walbraum–Cegarra syndrome
- Cryptorchidism-arachnodactyly-intellectual disability syndrome
- Curry–Jones syndrome
D
G
H
- H syndrome
- Hagemoser–Weinstein–Bresnick syndrome
- Hapnes Boman Skeie syndrome
- Hardcastle syndrome
- Heart-hand syndrome, Spanish type
- Hecht Scott syndrome
- Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome
- HIDEA syndrome
- Hirschsprung's disease-type D brachydactyly syndrome
- Holoprosencephaly-ectrodactyly-cleft lip/palate syndrome
- Huntington's disease-like syndrome
- Hypertension and brachydactyly syndrome
L
M
- Marsili syndrome
- MDP syndrome
- Meacham syndrome
- MEDNIK syndrome
- Menke-Hennekam syndrome
- Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome
- Microcephaly albinism digital anomalies syndrome
- Mirror polydactyly-vertebral segmentation-limb defects syndrome
- Morse–Rawnsley–Sargent syndrome
- Multicentric carpotarsal osteolysis syndrome
- Multiple congenital anomalies-hypotonia-seizures syndrome
- Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome
O
P
R
S
- Saal Greenstein syndrome
- Saito–Kuba–Tsuruta syndrome
- Sanjad–Sakati syndrome
- Santos–Mateus–Leal syndrome
- Say-Field-Coldwell syndrome
- Scalp defects-postaxial polydactyly syndrome
- SCARF syndrome
- Schwartz–Jampel syndrome
- Seaver–Cassidy syndrome
- Sengers syndrome
- SERKAL syndrome
- Sertoli cell-only syndrome
- Small patella syndrome
- Smith–Martin–Dodd syndrome
- Smith–Magenis syndrome
- Snijders Blok–Campeau syndrome
- Sotos syndrome
- Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
- Stimmler syndrome
- Stocco dos Santos syndrome
- Sudden infant death with dysgenesis of the testes syndrome
T
- Tel Hashomer camptodactyly syndrome
- Teunissen–Cremers syndrome
- Thai symphalangism syndrome
- Thumb stiffness-brachydactyly-intellectual disability syndrome
- Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome
- Tranebjaerg–Svejgaard syndrome
- Trigonocephaly-bifid nose-acral anomalies syndrome
- Triphalangeal thumbs-brachyectrodactyly syndrome
- Tucker syndrome