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Living with ITP
Information, shared experiences and research connections for people living with immune thrombocytopenia and those who support them.
Visit community Community liveLiving with ALPS
Information, shared experiences and research connections for people living with ALPS and those who support them.
Visit community Community liveLiving with ALS
Information, shared experiences and research connections for people living with ALS and those who support them.
Visit community Community liveLiving with Congenital myasthenic syndrome
Information, shared experiences and research connections for people living with congenital myasthenic syndrome and those who support them.
Visit community Community liveLiving with CVID
Information, shared experiences and research connections for people living with CVID and those who support them.
Visit community Community liveLiving with Cystic fibrosis
Information, shared experiences and research connections for people living with cystic fibrosis and those who support them.
Visit community Community liveLiving with Dermatomyositis
Information, shared experiences and research connections for people living with dermatomyositis and those who support them.
Visit community Community liveLiving with Fabry disease
Information, shared experiences and research connections for people living with Fabry disease and those who support them.
Visit community Community liveLiving with FMF
Information, shared experiences and research connections for people living with FMF and those who support them.
Visit community Community liveLiving with FSGS
Information, shared experiences and research connections for people living with FSGS and those who support them.
Visit community Community liveLiving with Gaucher disease
Information, shared experiences and research connections for people living with Gaucher disease and those who support them.
Visit community Community liveLiving with HAE (C1-INH)
Information, shared experiences and research connections for people living with HAE (C1-INH) and those who support them.
Visit community Community liveLiving with hEDS
Information, shared experiences and research connections for people living with hEDS and those who support them.
Visit community Community liveLiving with Huntington disease
Information, shared experiences and research connections for people living with Huntington disease and those who support them.
Visit community Community liveLiving with Myasthenia gravis
Information, shared experiences and research connections for people living with myasthenia gravis and those who support them.
Visit community Community liveLiving with Neonatal Marfan syndrome
Information, shared experiences and research connections for people living with Neonatal Marfan syndrome and those who support them.
Visit community Community liveLiving with PNH
Information, shared experiences and research connections for people living with PNH and those who support them.
Visit community Community liveLiving with Rett syndrome
Information, shared experiences and research connections for people living with Rett syndrome and those who support them.
Visit community Community liveLiving with SMA
Information, shared experiences and research connections for people living with SMA and those who support them.
Visit community Community liveLiving with Wilson disease
Information, shared experiences and research connections for people living with Wilson disease and those who support them.
Visit communityBrowse all 6,265 conditions
Every condition in the NIH Genetic and Rare Diseases Information Center has its own HealthSignal community page, with condition information, stories, research and Signals sign-up.
653 conditions starting with A
- A20 haploinsufficiency
- AA amyloidosis
- Aase-Smith syndrome
- Abdominal cystic lymphangioma
- Abetalipoproteinaemia
- Ablepharon macrostomia syndrome
- Abortive cerebellar ataxia
- ABri amyloidosis
- Abruzzo-Erickson syndrome
- Absence deformity of leg-cataract syndrome
- Absent foot
- Absent hand
- Absent radius-anogenital anomalies syndrome
- Absent septum pellucidum
- Absent tibia-polydactyly-arachnoid cyst syndrome
- Acalvaria
- Acanthamoeba keratitis
- Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome
- Acatalasia
- Accessory pancreas
- Achalasia microcephaly syndrome
- Acheiropodia
- Achondrogenesis
- Achondrogenesis, type IB
- Achondroplasia
- Achromatopsia
- Achromatopsia 2
- Achromatopsia 3
- Achromatopsia 6
- Acid phosphatase deficiency
- Acid sphingomyelinase deficiency
- Ackerman syndrome
- Acoustic neuroma
- Acquired adult-onset immunodeficiency
- Acquired angioedema
- Acquired epidermolysis bullosa
- Acquired factor VIII deficiency disease
- Acquired generalized lipodystrophy
- Acquired hemoglobin H disease
- Acquired hemophilia
- Acquired hypertrichosis lanuginosa
- Acquired idiopathic inflammatory myopathy
- Acquired partial lipodystrophy
- Acquired polycythemia vera
- Acquired thrombotic thrombocytopenic purpura
- Acquired von willebrand syndrome
- Acral peeling skin syndrome
- Acral self-healing collodion baby
- Acro-renal-mandibular syndrome
- Acrocallosal syndrome
- Acrocapitofemoral dysplasia
- Acrocardiofacial syndrome
- Acrocephalopolydactyly
- Acrocephalosyndactyly type I
- Acrocephalosyndactyly type V
- Acrocraniofacial dysostosis
- Acrodysostosis
- Acroerythrokeratoderma
- Acrofacial dysostosis Rodriguez type
- Acrofacial dysostosis, Catania type
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