ACROCEPHALOSYNDACTYLY TYPE III
ACROCEPHALOSYNDACTYLY TYPE V
ACRODYSOSTOSIS
ACYL-CoA DEHYDROGENASE, LONG-CHAIN, DEFICIENCY OF
ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF
ADRENAL HYPERPLASIA I
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
ALBINISM I
ALBINISM II
ALPHA-METHYLACETOACETICACIDURIA
AMAUROSIS CONGENITA OF LEBER I
AMAUROTIC FAMILY IDIOCY, JUVENILE TYPE
ANGIONEUROTIC EDEMA, HEREDITARY
ANUS, IMPERFORATE, WITH HAND, FOOT AND EAR ANOMALIES
ARGININOSUCCINICACIDURIA
ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH PULMONARY HYPOPLASIA
ASPLENIA WITH CARDIOVASCULAR ANOMALIES
BIRD-HEADED DWARFISM, OSTEODYSPLASTIC TYPE I
BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS
BRANCHIOOTORENAL DYSPLASIA
CAMPTODACTYLY, CLEFT PALATE, AND CLUBFOOT
CEREBRAL GIGANTISM
CHOANAL ATRESIA, POSTERIOR
CLEFT LIP AND/OR PALATE WITH MUCOUS CYSTS OF LOWER LIP
CONSTRICTING BANDS, CONGENITAL
CONVULSIONS, BENIGN FAMILIAL NEONATAL
CRANIOFRONTONASAL DYSPLASIA
DEAFNESS, CONGENITAL, I
DEAFNESS, DOMINANT CONGENITAL SEVERE SENSORINEURAL
DEAFNESS, PROGRESSIVE HIGH-TONE NEURAL
dermatologic disease
DIASTROPHIC DYSPLASIA
DUBOWITZ SYNDROME
ECTODERMAL DYSPLASIA, HIDROTIC
ECTODERMAL DYSPLASIA, HYPOHIDROTIC
FEMORAL-FACIAL SYNDROME
FG SYNDROME
FRYNS SYNDROME
GALACTOKINASE DEFICIENCY
GAUCHER DISEASE, TYPE I
GLUTARICACIDEMIA I
GLUTARICACIDURIA IIB
GLYCINEMIA, KETOTIC, I
GLYCINEMIA, KETOTIC, II
head disease
HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES
HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS
HEMOGLOBIN--BETA LOCUS
HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS
HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION
HYDROXYACYL-CoA DEHYDROGENASE
HYPERAMMONEMIA DUE TO CARBAMOYLPHOSPHATE SYNTHETASE I DEFICIENCY
HYPERPARATHYROIDISM, FAMILIAL PRIMARY
HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS
HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME
HYPOPHOSPHATASIA, CHILDHOOD
INTESTINAL ATRESIA, MULTIPLE
ISOVALERICACIDEMIA
JOHANSON-BLIZZARD SYNDROME
JOINT CONTRACTURES WITH OTHER ABNORMALITIES
KBG SYNDROME
KLIPPEL-FEIL DEFORMITY, DEAFNESS, AND FACIAL ASYMMETRY
LACTIC ACIDOSIS, CONGENITAL INFANTILE
LARSEN SYNDROME, DOMINANT
MACROCEPHALY, BENIGN FAMILIAL
MAXILLONASAL DYSPLASIA, BINDER TYPE
MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 1
METAPHYSEAL CHONDRODYSPLASIA, MCKUSICK TYPE
METHYLMALONICACIDURIA DUE TO METHYLMALONIC CoA MUTASE DEFICIENCY
METHYLMALONICACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN--cbl A
METHYLMALONICACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN--cbl B
MICROCEPHALY, AUTOSOMAL DOMINANT
MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES
MUCOPOLYSACCHARIDOSIS TYPE IIIA
MUCOPOLYSACCHARIDOSIS TYPE IIIB
MUCOPOLYSACCHARIDOSIS TYPE IVA
MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE AND BECKER TYPES
Musculoskeletal and connective tissue disorder
MYOPATHY, CENTRONUCLEAR
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION
neck disease
NEUROFIBROMATOSIS, TYPE IV, OF RICCARDI
Neurofibromatosis, unspecified
NIEMANN-PICK DISEASE, TYPE C
OLIVOPONTOCEREBELLAR ATROPHY I
OSTEOCHONDROSIS DEFORMANS TIBIAE, FAMILIAL INFANTILE TYPE
OSTEOGENESIS IMPERFECTA WITH BLUE SCLERAE
otorhinolaryngologic disease
peritoneal disease
POLYDACTYLY, POSTAXIAL
POLYSYNDACTYLY WITH PECULIAR SKULL SHAPE
PSEUDOACHONDROPLASTIC DYSPLASIA I
PTOSIS, HEREDITARY CONGENITAL
RETINITIS PIGMENTOSA-1
retroperitoneal disease
RIEGER SYNDROME
RUSSELL-SILVER SYNDROME, X-LINKED
RUTLEDGE LETHAL MULTIPLE CONGENITAL ANOMALY SYNDROME
SCHIZOPHRENIA-1
soft tissue disease
Connective and Soft Tissue Neoplasm
Bone neoplasms
Mesenchymal Cell Neoplasm
Benign Mesenchymal Cell Neoplasm
Chondrogenic Neoplasm
Miscellaneous Mesenchymal Neoplasm
Notochordal Tumor
Osteogenic Neoplasm
Perivascular Tumor
Soft Tissue Neoplasms
Benign Neoplasm of Soft Tissue
Breast Soft Tissue Tumor
Cervical Soft Tissue Tumor
Extraskeletal Cartilaginous and Osseous Tumor
Fallopian Tube Soft Tissue Neoplasm
Myomatous neoplasm
Neoplasm of the Synovium
Neoplasms in Vascular Tissue
Neoplasms, Connective Tissue
Sarcoma
Skin Neoplasms
Soft Tissue Neoplasm of Central Nervous System
Soft Tissue Neoplasm of the Ovary
Stromal Neoplasm
Uterine Corpus Soft Tissue Neoplasm
Vaginal Soft Tissue Tumor
Vulvar Soft Tissue Tumor
Musculoskeletal Malfunction Arising from Mental Factor
Neoplasms, Muscle Tissue
Non-Neoplastic Soft Tissue Disorder
Rheumatism
Skin and subcutaneous tissue disease
Soft Tissue Infections
SPASTIC PARAPLEGIA
SPONDYLOEPIPHYSEAL DYSPLASIA, LATE
stomatognathic system disease
SYNOSTOSES, TARSAL, CARPAL AND DIGITAL
THROMBOCYTOPENIA--ABSENT RADIUS SYNDROME
TRICHORHINOPHALANGEAL SYNDROME, TYPE I
UROGENITAL ADYSPLASIA, HEREDITARY
VASCULITIS, HEREDITARY INFLAMMATORY, WITH PERSISTENT NODULES
VATER ASSOCIATION
VERTEBRAL ANOMALIES
WEAVER-LIKE SYNDROME | Preferred Name | Melanoma |
| Synonyms | "Malignant melanoma, morphology (morphologic abnormality)" "melanoma" "[M]Malignant melanoma NOS (morphologic abnormality)" "[M]Naevocarcinoma" "MALIGNANT MELANOMA" "Malignant Melanoma" "Malignant melanoma" "Malignant melanoma (disorder)" |
| ID | DOID:1909 |
| Full Id | |
| Database References |
UMLS_ST |
| Exact Synonym |
"Malignant melanoma, morphology (morphologic abnormality)" "melanoma" "[M]Malignant melanoma NOS (morphologic abnormality)" "[M]Naevocarcinoma" "MALIGNANT MELANOMA" "Malignant Melanoma" "Malignant melanoma" "Malignant melanoma (disorder)" |
| Xref Exact Synonym |
SNOMEDCT_2005_07_31:2092003 CSP2005:2020-2434 MTH:NOCODE SNOMEDCT_2005_07_31:269503007 SNOMEDCT_2005_07_31:189749008 MTH:475 NCI2004_11_17:C3224 SNOMEDCT_2005_07_31:154501005 SNOMEDCT_2005_07_31:269577007 SNOMEDCT_2005_07_31:372244006 |
| Is A |
| Subject | Subject Sort | Archive Sort | Author | Type | Target | Created |
|---|---|---|---|---|---|---|
| Wikipedia page for melanoma | Wikipedia page for melanoma | false | mmontegut | Comment | Melanoma (Class) | 07/21/2008 |
| Subject | Subject Sort | Archive Sort | Author | Type | Target | Created |
|---|
loading...
loading...
loading...
loading...