Age related macular degeneration 4 is a condition where changes in the eye's macula are linked to a mutation in the CFH gene. This form of macular deg...

Age related macular degeneration 6 is a form of age-related macular degeneration linked to a mutation in the RAX2 gene. This condition is defined by c...

Age related macular degeneration 7 is a form of age-related macular degeneration where a mutation in the HTRA1 gene plays a key role. This condition a...

Age related macular degeneration 8 is a condition where a change in the ARMS2 gene leads to vision problems associated with age-related macular degene...

Age related macular degeneration 9 is a type of macular degeneration where changes occur in the central part of the retina due to a mutation in the C3...

Aggressive B-cell non-Hodgkin lymphoma is a type of cancer affecting the lymphatic system, where abnormal lymphocytes grow rapidly and can spread to o...

Aggressive NK-cell leukemia is a rare and highly aggressive blood cancer that is associated with the Epstein-Barr virus. It is also known as aggressiv...

Aggressive systemic mastocytosis (ASM) is a severe and rare form of systemic mastocytosis. In this condition, there is a significant buildup of mast c...

Agnathia-holoprosencephaly-situs inversus syndrome is an extremely rare condition characterized by the absence of the mandible along with brain malfor...

Agranulocytosis is a condition where there is a decrease in the number of mature granulocytes in the peripheral blood. Granulocytes include neutrophil...

AH amyloidosis, also known as heavy chain amyloidosis, is a condition characterized by the abnormal deposition of protein fragments in tissues, althou...

AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome is a developmental disorder that primarily affects the ner...

Aicardi-Goutieres syndrome (AGS) is an inherited subacute encephalopathy that primarily affects the brain, characterized by basal ganglia calcificatio...

Aicardi-Goutieres syndrome 1 is a severe early-onset encephalopathy that primarily affects the central nervous system and is characterized by extensiv...

Aicardi-Goutieres syndrome 2 is an inherited neurodevelopmental condition that primarily affects the nervous system, causing early-onset encephalopath...

Aicardi-Goutieres syndrome 3 is a rare genetic disorder caused by a mutation in the RNASEH2C gene. It is one of the forms of Aicardi-Goutieres syndrom...

Aicardi-Goutieres syndrome 4 is a neurodevelopmental condition primarily affecting brain function and characterized by an early-onset encephalopathy w...

Aicardi-Goutieres syndrome 5 is a congenital neuroinflammatory condition that primarily affects the central nervous system, manifesting as an early-on...

Aicardi-Goutieres syndrome 6 is a genetically determined condition that primarily affects neurological development and involves aspects of immune regu...

Aicardi-Goutieres syndrome 7 is an inherited neuroinflammatory encephalopathy that primarily affects the brain and other organ systems including blood...