Category:Rare syndromes
From WikiMD's Wellness Encyclopedia
Pages in category "Rare syndromes"
The following 200 pages are in this category, out of 209 total.
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A
- Acrocallosal syndrome, Schinzel type
- Adenosine Deaminase 2 deficiency
- Aicardi syndrome
- Alagille Syndrome
- Alagille syndrome
- Alezzandrini syndrome
- Alien hand syndrome
- Alpers disease
- Alström syndrome
- Andersen–Tawil syndrome
- Angelman syndrome
- Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges
- ANOTHER syndrome
- Hypohidrotic ectodermal dysplasia with hypothyroidism and ciliary dyskinesia
- Antisynthetase syndrome
- Apert syndrome
- Apparent mineralocorticoid excess syndrome
- Aromatase excess syndrome
- Arterial tortuosity syndrome
- Arts syndrome
B
- Bannayan-Riley-Ruvalcaba syndrome
- Barakat syndrome
- Bardet-Biedl syndrome
- Barraquer-Simons syndrome
- Barth syndrome
- Bartter syndrome
- Bartter syndrome type 3
- Beckwith–Wiedemann syndrome
- Giant platelet syndrome
- Birt-Hogg-Dube syndrome
- Bjornstad syndrome
- Bloom syndrome
- Blue diaper syndrome
- Blue rubber bleb nevus syndrome
- Wyburn-Mason syndrome
- Borjeson-Forssman-Lehmann syndrome
- Bowen-Conradi syndrome
- Branchiooculofacial syndrome
- Branchiootorenal syndrome
- Riboflavin transporter deficiency
- Bruck syndrome
- Bruck syndrome 1
- Brugada syndrome
- Budd-Chiari syndrome
C
- Cantú syndrome
- Carey-Fineman-Ziter syndrome
- Carpenter syndrome
- Cat eye syndrome
- Caudal regression sequence
- Central hypoventilation syndrome
- CHILD syndrome
- Christianson syndrome
- Chromosome 1p duplication
- Chromosome 1q21.1 duplication syndrome
- Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature
- CLOVES syndrome
- Cohen syndrome
- Cone-rod dystrophy amelogenesis imperfecta
- Congenital generalized lipodystrophy
- Congenital generalized lipodystrophy type 1
- Congenital intrauterine infection-like syndrome
- Cornelia de Lange syndrome
- Costello syndrome
- Cowden syndrome
- Cranioectodermal dysplasia
- Crigler-Najjar syndrome
- Crigler–Najjar syndrome
- Crome syndrome
- Crouzon syndrome
- Cryopyrin associated periodic syndromes
- Cryopyrin-associated periodic syndrome
- Currarino triad
D
F
G
H
I
K
L
M
- Mal de debarquement syndrome
- Marden–Walker syndrome
- Marfan syndrome
- Maroteaux–Lamy syndrome
- McLeod neuroacanthocytosis syndrome
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
- Mitochondrial DNA-associated Leigh syndrome
- Monoamine oxidase A deficiency
- Morquio syndrome
- Mucopolysaccharidosis type IVA
- MPV17-related hepatocerebral mitochondrial DNA depletion syndrome
- Myoclonic epilepsy with ragged red fibers
N
O
P
- Pallister-Killian mosaic syndrome
- Papillon Lefevre syndrome
- Blepharonasofacial malformation syndrome
- Pearson syndrome
- PEHO syndrome
- Peters plus syndrome
- PIK3CA-related overgrowth spectrum
- POEMS syndrome
- Poland syndrome
- Pontocerebellar hypoplasia
- Pontocerebellar hypoplasia type 1
- Pontocerebellar hypoplasia type 2
- Pontocerebellar hypoplasia type 3
- Pontocerebellar hypoplasia type 4
- Pontocerebellar hypoplasia type 5
- Pontocerebellar hypoplasia type 6
- Popliteal pterygium syndrome
- Proteus syndrome
