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255399007: Congenital (qualifier value)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
380598010 Congenital en Synonym Active Entire term case insensitive SNOMED CT core module
380599019 Congenita en Synonym Active Entire term case insensitive SNOMED CT core module
646433016 Congenital (qualifier value) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital Is a Periods of life true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital sixth nerve palsy Occurrence False Congenital Inferred relationship Existential restriction modifier
Cryptophthalmos Occurrence False Congenital Inferred relationship Existential restriction modifier
Ankyloblepharon filiforme adnatum Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital tarsal kink Occurrence False Congenital Inferred relationship Existential restriction modifier
Euryblepharon Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital miosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital mydriasis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital iris ectropion Occurrence False Congenital Inferred relationship Existential restriction modifier
Dysplasia of cerebral cortex Occurrence False Congenital Inferred relationship Existential restriction modifier
Nicolaides-Baraitser syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Pena-Shokeir syndrome type I Occurrence False Congenital Inferred relationship Existential restriction modifier
Smith-Magenis syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Epidermolysis bullosa acquisita, classical acral type Occurrence False Congenital Inferred relationship Existential restriction modifier
Epidermolysis bullosa acquisita, bullous pemphigoid-like Occurrence False Congenital Inferred relationship Existential restriction modifier
Epidermolysis bullosa acquisita, cicatricial pemphigoid-like Occurrence False Congenital Inferred relationship Existential restriction modifier
Epidermolysis bullosa acquisita, Brunsting-Perry type Occurrence False Congenital Inferred relationship Existential restriction modifier
Epidermolysis bullosa acquisita, oral mucosal involvement Occurrence False Congenital Inferred relationship Existential restriction modifier
Tophus co-occurrent and due to gout Occurrence False Congenital Inferred relationship Existential restriction modifier
Tophus of digit co-occurrent and due to gout Occurrence False Congenital Inferred relationship Existential restriction modifier
Sporadic porphyria cutanea tarda Occurrence False Congenital Inferred relationship Existential restriction modifier
Immunodeficiency with multicarboxylase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Congenital malignant melanoma Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital vascular malformation of skin Occurrence False Congenital Inferred relationship Existential restriction modifier
Acquired cutaneous vascular malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Developmental anomaly of vitelline duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal dominant ichthyosis Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked recessive ichthyosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal recessive ichthyosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Punctate palmoplantar keratoderma Occurrence False Congenital Inferred relationship Existential restriction modifier
Genetic defect of hair shaft Occurrence False Congenital Inferred relationship Existential restriction modifier
Inherited epidermolysis bullosa Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital/hereditary cutis laxa Occurrence False Congenital Inferred relationship Existential restriction modifier
Genetic disorder of lipid storage Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital vascular malformation due to inherited syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Developmental malformation of branchial arch Occurrence False Congenital Inferred relationship Existential restriction modifier
Acquired arteriovenous malformation of the skin Occurrence False Congenital Inferred relationship Existential restriction modifier
Fordyce spots of lips Occurrence False Congenital Inferred relationship Existential restriction modifier
Fordyce spots of buccal mucosa Occurrence False Congenital Inferred relationship Existential restriction modifier
Fordyce spots of penis Occurrence False Congenital Inferred relationship Existential restriction modifier
Fordyce spots of vulva Occurrence False Congenital Inferred relationship Existential restriction modifier
Post-inflammatory cutis laxa Occurrence False Congenital Inferred relationship Existential restriction modifier
Cutis laxa following urticaria-angioedema Occurrence False Congenital Inferred relationship Existential restriction modifier
Cutis laxa following hypersensitivity reaction Occurrence False Congenital Inferred relationship Existential restriction modifier
Cutis laxa with complement deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Solitary infantile myofibromatosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Multicentric infantile myofibromatosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Aggressive systemic infantile myofibromatosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital lower lip pits Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary mucoepithelial dysplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Patent vitelline duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Vitelline duct polyp Occurrence False Congenital Inferred relationship Existential restriction modifier
Hypertrichosis with congenital macrogingivae Occurrence False Congenital Inferred relationship Existential restriction modifier
Vertical alopecia Occurrence False Congenital Inferred relationship Existential restriction modifier
Sutural alopecia Occurrence False Congenital Inferred relationship Existential restriction modifier
Triangular alopecia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital pigmented nevus with atypical melanocytic proliferation Occurrence False Congenital Inferred relationship Existential restriction modifier
Port-wine stain with associated anomalies Occurrence False Congenital Inferred relationship Existential restriction modifier
Port-wine stain with oculocutaneous melanosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Aplasia cutis congenita due to underlying malformation (Type 4) Occurrence False Congenital Inferred relationship Existential restriction modifier
Aplasia cutis congenita associated with fetus papyraceus (Type 5) Occurrence False Congenital Inferred relationship Existential restriction modifier
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) Occurrence False Congenital Inferred relationship Existential restriction modifier
Aplasia cutis congenita due to teratogenic drug (Type 7) Occurrence False Congenital Inferred relationship Existential restriction modifier
Aplasia cutis congenita following intra-uterine infection (Type 8) Occurrence False Congenital Inferred relationship Existential restriction modifier
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Occurrence False Congenital Inferred relationship Existential restriction modifier
Oculocerebrocutaneous syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Midline cervical cleft Occurrence False Congenital Inferred relationship Existential restriction modifier
Cutaneous lesion resulting from spinal dysraphism Occurrence False Congenital Inferred relationship Existential restriction modifier
Port-wine stain associated with spinal dysraphism Occurrence False Congenital Inferred relationship Existential restriction modifier
Cutaneous lesion resulting from spina bifida Occurrence False Congenital Inferred relationship Existential restriction modifier
Rudimentary digit Occurrence False Congenital Inferred relationship Existential restriction modifier
Drug-induced epidermolysis bullosa acquisita Occurrence False Congenital Inferred relationship Existential restriction modifier
Drug-induced cutis laxa Occurrence False Congenital Inferred relationship Existential restriction modifier
Pseudoporphyria due to psoralen and long-wave ultraviolet radiation therapy Occurrence False Congenital Inferred relationship Existential restriction modifier
Hemodialysis-associated pseudoporphyria Occurrence False Congenital Inferred relationship Existential restriction modifier
Porphyria-like reaction caused by poison and/or environmental toxin Occurrence False Congenital Inferred relationship Existential restriction modifier
Porphyria caused by hexachlorobenzene Occurrence False Congenital Inferred relationship Existential restriction modifier
Porphyria caused by chlorinated phenol Occurrence False Congenital Inferred relationship Existential restriction modifier
Aplasia cutis in Trisomy 13 syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) Occurrence False Congenital Inferred relationship Existential restriction modifier
Café-au-lait spots and ring chromosome 11 Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal chromosomal disorder Occurrence False Congenital Inferred relationship Existential restriction modifier
XXYY syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Poly Y syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Odonto-onycho-dermal dysplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Aplasia cutis in Johanson-Blizzard syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Odontomicronychial ectodermal dysplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Port-wine stain in Rubinstein-Taybi syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma Occurrence False Congenital Inferred relationship Existential restriction modifier
Cardio-acral-facial syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Cardio-facio-cutaneous syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Bitemporal scars with abnormal eyelashes Occurrence False Congenital Inferred relationship Existential restriction modifier
Cleft palate lateral synechia syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Facial milia, lobate tongue, lingual and labial frenula syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary neurocutaneous angiomata Occurrence False Congenital Inferred relationship Existential restriction modifier
Lamellar ichthyosis (limited type) Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked dominant chondrodysplasia punctata of Happle Occurrence False Congenital Inferred relationship Existential restriction modifier
Ichthyosis, cerebellar degeneration and hepatosplenomegaly Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal recessive keratitis-ichthyosis-deafness syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Ichthyosis follicularis with alopecia and photophobia Occurrence False Congenital Inferred relationship Existential restriction modifier
Flexural Darier's disease Occurrence False Congenital Inferred relationship Existential restriction modifier

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