Pages that link to "Q10267817"
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The following pages link to autosomal recessive disease (Q10267817):
Displaying 50 items.
- Norman–Roberts syndrome (Q130555) (← links)
- Lafora disease (Q163905) (← links)
- cystic fibrosis (Q178194) (← links)
- sickle-cell disease (Q185034) (← links)
- thalassemia (Q185137) (← links)
- prune belly syndrome (Q250354) (← links)
- Schindler disease (Q310335) (← links)
- abetalipoproteinemia (Q319812) (← links)
- aceruloplasminemia (Q337604) (← links)
- Alström syndrome (Q432814) (← links)
- glycogen storage disease III (Q494922) (← links)
- sucrose intolerance (Q498826) (← links)
- congenital insensitivity to pain with anhidrosis (Q501694) (← links)
- trimethylaminuria (Q506433) (← links)
- Seckel syndrome (Q572169) (← links)
- Dubowitz syndrome (Q574741) (← links)
- Antley-Bixler syndrome (Q585011) (← links)
- xeroderma pigmentosum (Q612693) (← links)
- Roberts syndrome (Q619428) (← links)
- ectrodactyly (Q650026) (← links)
- TAR syndrome (Q660330) (← links)
- Laron syndrome (Q669822) (← links)
- neurogenic arthrogryposis multiplex congenita (Q708165) (← links)
- asplenia with cardiovascular anomalies (Q772022) (← links)
- Behr syndrome (Q814547) (← links)
- Bernard-Soulier syndrome (Q822228) (← links)
- Cockayne syndrome (Q914389) (← links)
- Usher syndrome (Q917399) (← links)
- Chediak-Higashi syndrome (Q934034) (← links)
- epidermodysplasia verruciformis (Q974691) (← links)
- inherited pseudoxanthoma elasticum (Q1052391) (← links)
- Gitelman syndrome (Q1053120) (← links)
- cystinosis (Q1149042) (← links)
- leukocyte-adhesion deficiency syndrome (Q1154422) (← links)
- Werner syndrome (Q1154619) (← links)
- DOOR syndrome (Q1154764) (← links)
- Nijmegen breakage syndrome (Q1250362) (← links)
- nephronophthisis (Q1257011) (← links)
- Dyggve–Melchior–Clausen syndrome (Q1268671) (← links)
- sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome (Q1313757) (← links)
- congenital muscular dystrophy (Q1321884) (← links)
- Ellis–Van Creveld syndrome (Q1332448) (← links)
- sitosterolemia (Q1336034) (← links)
- Fazio-Londe disease (Q1399155) (← links)
- Fraser syndrome (Q1425572) (← links)
- pantothenate kinase-associated neurodegeneration (Q1436162) (← links)
- Bloom syndrome (Q1469646) (← links)
- gangliosidosis (Q1493513) (← links)
- Hermansky-Pudlak syndrome (Q1506216) (← links)
- hereditary folate malabsorption (Q1609733) (← links)