Category:Genetic syndromes
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Subcategories
This category has the following 2 subcategories, out of 2 total.
G
- Genetic anomalies (1 C, 22 P)
R
- Rare genetic syndromes (1 C, 166 P)
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
- 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
- Hapnes Boman Skeie 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
W
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