CO COA COB COC COD COE COF COG COH COI COK COL COM CON COO COP COQ COR COS COT COU COV COW COX COY COZ
CONG ECTODERMAL DYSPLAS
[A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, FOCAL DERMAL HYPOPLASIA, and aplasia cutis congenita. ( MSH )]
UMLS (ICD9CM) C0013575- Congenital Abnormality
- Disease or Syndrome
Relation/PAR: Abnormalities, Multiple
Sex Chromosome Abnormalities
Congenital anomalies of the integument
Sex Chromosome Abnormalities
Congenital anomalies of the integument
Relation/CHD: CHONDROECTODERM DYSPLAS
focal dermal hypoplasia
Neurocutaneous Syndromes
focal dermal hypoplasia
Neurocutaneous Syndromes
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