Disease Index

Human disease

N-acetylglutamate synthase (NAGS) deficiency is a urea cycle disorder leading to hyperammonaemia

The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome is a rare microdeletion syndrome associated with a distinct facial appearance.

Naegeli-Franceschetti-Jadassohn (NFJ) syndrome is a rare ectodermal dysplasia that affects the skin, sweat glands, nails, and teeth

acrofacial dysostosis characterized by underdeveloped cheek bones, very small lower jaw, cleft palate, defects in the middle ear, absent eyelashes, and a notch in the lower eyelids called a coloboma, in children

epidermal appendage anomaly that involves the nail

Human disease

Nail-patella-like renal disease is a severe nephropathy characterised by renal dysfunction, proteinuria, oedema and microscopic haematuria. It has been described in three brothers, two of which died from end-stage renal insufficiency.

syndrome

disorder of lens

Narcolepsy without cataplexy is characterized by excessive day-time sleepiness associated with uncontrollable sleep urges and sometimes paralysis at sleep, hypnagogic hallucinations and automatic behavior

Narcolepsy with cataplexy is a sleep disorder characterized by excessive day-time sleepiness associated with uncontrollable sleep urges and cataplexy (loss of muscle tone often triggered by pleasant emotions)

human disease

human disease

Glioma is a nipped off portion of encephalocele during embryoninc development .It may b extranasal and intranasal

Rare X-linked recessive genetic syndrome

medical condition

Nasopalpebral lipoma-coloboma-telecanthus syndrome is characterized by nasopalpebral lipomas, bilateral lid coloboma, and telecanthus

medical condition

teratoma that involves the nasopharynx

common cancer originating in the nasopharynx

human disease

human disease

medical condition

Human disease

Human disease