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Longer titles found: Aplasia cutis congenita-intestinal lymphangiectasia syndrome (view)

searching for Aplasia cutis congenita 7 found (20 total)

alternate case: aplasia cutis congenita

Charcot–Marie–Tooth disease (4,443 words) [view diff] no match in snippet view article find links to article

Charcot–Marie–Tooth disease (CMT) is a hereditary motor and sensory neuropathy of the peripheral nervous system characterized by progressive loss of muscle
Focal facial dermal dysplasia (570 words) [view diff] exact match in snippet view article find links to article
symmetrical aplastic nevi of temples, bitemporal aplasia cutis congenita, bitemporal aplasia cutis congenita: OMIM 136500) and Setleis syndrome (facial ectodermal
Bart syndrome (293 words) [view diff] exact match in snippet view article find links to article
Bart syndrome, also known as aplasia cutis congenita type VI, is a rare genetic disorder characterized by the association of congenital localized absence
Adams–Oliver syndrome (1,952 words) [view diff] exact match in snippet view article find links to article
the limbs, and mottling of the skin. Two key features of AOS are aplasia cutis congenita with or without underlying bony defects and terminal transverse
Rivka Carmi (2,526 words) [view diff] exact match in snippet view article find links to article
is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients". American Journal of Medical
List of diseases (M) (2,469 words) [view diff] exact match in snippet view article
dysautonomia Motor neuropathy Motor sensory neuropathy type 1 aplasia cutis congenita Mounier-Kuhn syndrome Mount–Reback syndrome Mousa Al din Al Nassar
List of diseases (C) (3,648 words) [view diff] exact match in snippet view article
disease deafness recessive type Charcot–Marie–Tooth disease type 1 aplasia cutis congenita Charcot–Marie–Tooth disease type 1A Charcot–Marie–Tooth disease