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searching for Gordon syndrome 8 found (14 total)

Palmoplantar keratoderma (2,035 words) [view diff] no match in snippet view article find links to article

Palmoplantar keratodermas are a heterogeneous group of skin disorders characterized by abnormal thickening (scleroderma) of the stratum corneum of the

SYT1-associated neurodevelopmental disorder (314 words) [view diff] exact match in snippet view article find links to article

SYT1-associated neurodevelopmental disorder, also known as Baker-Gordon syndrome, is a rare genetic disorder caused by mutations in the synaptotagmin-1

WNK4 (3,448 words) [view diff] exact match in snippet view article find links to article

cause a genetic form of pseudohypoaldosteronism type 2, also called Gordon syndrome or Familial Hyperkalemic Hypertension. WNK4 is a member of a serine/threonine

ANKRD17 (571 words) [view diff] exact match in snippet view article find links to article

gene. De novo mutations to ANKRD17 are known to cause Chopra-Amiel-Gordon syndrome. Genetic analysis of individuals with CAGS suggests that the disorder

Pseudohypoaldosteronism (2,139 words) [view diff] exact match in snippet view article find links to article

infertility. PHA2 also known as Familial hyperkalemic hypertension or Gordon syndrome is a rare disorder characterized by abnormalities in how the body regulates

SYT1 (1,503 words) [view diff] case mismatch in snippet view article find links to article

disorder known as SYT1-associated neurodevelopmental disorder (or Baker-Gordon Syndrome). GRCh38: Ensembl release 89: ENSG00000067715 – Ensembl, May 2017 GRCm38:

List of diseases (G) (846 words) [view diff] exact match in snippet view article

Goodpasture's syndrome Gordon hyperkaliemia-hypertension syndrome Gordon syndrome Gorham syndrome Gorham's disease Gorham–Stout disease Gorlin–Bushkell–Jensen

List of diseases (P) (1,908 words) [view diff] exact match in snippet view article

Powell–Buist–Stenzel syndrome Powell–Chandra–Saal syndrome Powell–Venencie–Gordon syndrome Poxviridae disease Prader–Willi syndrome Prata–Liberal–Goncalves syndrome