Rare Disease Library

Gabriele-de Vries syndrome

YY1 haploinsufficiency syndrome

Combined immunodeficiency due to RELA haploinsufficiency

RELA-associated inflammatory disease · CID due to RELA haploinsufficiency

Creatine deficiency syndrome

CDS · Cerebral creatine deficiency syndrome

Early-onset autoinflammatory syndrome due to A20 haploinsufficiency

Early-onset AID due to HA20 · Early-onset autoinflammatory disorder due to HA20

Familial hyperinflammatory lymphoproliferative immunodeficiency

NCKAP1L-associated hyperinflammatory disorder · HEM1 deficiency syndrome

Familial steroid-resistant nephrotic syndrome with adrenal insufficiency

SPLIS · Primary adrenal insufficiency-steroid-resistant nephrotic syndrome due to SGPL1 deficiency

Immune dysregulation-inflammatory bowel disease- recurrent sinopulmonary infections syndrome

NFAT5 haploinsufficiency

Intellectual disability-expressive aphasia-facial dysmorphism syndrome

SETBP1 haploinsufficiency disorder · Intellectual disability-loss of expressive language-facial dysmorphism syndrome

Lamb-Shaffer syndrome

SOX5 haploinsufficiency syndrome

PDE4D haploinsufficiency syndrome

Rh deficiency syndrome

Rh-null syndrome

Rubinstein-Taybi syndrome due to EP300 haploinsufficiency

Severe intellectual disability and progressive spastic paraplegia

AP4 deficiency syndrome

Triple A syndrome

2A syndrome · 3A syndrome

X-linked central congenital hypothyroidism with late-onset testicular enlargement

IGSF1 deficiency syndrome · X-linked central congenital hypothyroidism with late-onset macroorchidism

X-linked lymphoproliferative disease due to XIAP deficiency

X-linked lymphoproliferative syndrome type 2 · XLP2