Webbed neck
Symptom Information:
Symptom ID: | HPO:0000465 | |||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of head or neck(HPO:0000152) Abnormality of the neck(HPO:0000464) Webbed neck(HPO:0000465) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396) Musculoskeletal and connective tissue disorders of face, neck and jaw congenital(MedDRA:10028380) Webbed neck(HPO:0000465) |
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Database Frequency: | 81 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
Acrofacial dysostosis, Catania type | (Orphanet:1786) |
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
BARAITSER-WINTER SYNDROME 2 | (OMIM:614583) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Blackfan-Diamond anemia | (Orphanet:124) |
CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III | (OMIM:611929) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CHARGE syndrome | (Orphanet:138) |
CHROMOSOME 17p13.1 DELETION SYNDROME | (OMIM:613776) |
CREE MENTAL RETARDATION SYNDROME | (OMIM:606851) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cerebro-costo-mandibular syndrome | (Orphanet:1393) |
Costello syndrome | (Orphanet:3071) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniosynostosis - fibular aplasia | (Orphanet:1533) |
Craniosynostosis, Herrmann-Opitz type | (Orphanet:2145) |
DIAMOND-BLACKFAN ANEMIA 1 | (OMIM:105650) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Diaphanospondylodysostosis | (Orphanet:66637) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Distal monosomy 10p | (Orphanet:1580) |
Distal monosomy 10q | (Orphanet:96148) |
Dysmorphism - multiple structural anomalies | (Orphanet:1780) |
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS | (OMIM:227255) |
Frontonasal dysplasia | (Orphanet:250) |
Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
Intellectual deficit, X-linked, Snyder type | (Orphanet:3063) |
Isolated Klippel-Feil syndrome | (Orphanet:2345) |
Jacobsen syndrome | (Orphanet:2308) |
KERATOCONUS POSTICUS CIRCUMSCRIPTUS | (OMIM:244600) |
LEOPARD SYNDROME 1 | (OMIM:151100) |
LEOPARD SYNDROME 2 | (OMIM:611554) |
LEOPARD SYNDROME 3 | (OMIM:613707) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
Lethal congenital contracture syndrome type 1 | (Orphanet:1486) |
Lethal multiple pterygium syndrome | (Orphanet:33108) |
Lymphedema - distichiasis | (Orphanet:33001) |
MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Microcephaly - cardiac defect - lung malsegmentation | (Orphanet:2516) |
Microphthalmia, Lenz type | (Orphanet:568) |
Monosomy 13q14 | (Orphanet:1587) |
Monosomy 9p | (Orphanet:261112) |
Mosaic trisomy 9 | (Orphanet:99776) |
NOONAN SYNDROME 1 | (OMIM:163950) |
NOONAN SYNDROME 3 | (OMIM:609942) |
NOONAN SYNDROME 4 | (OMIM:610733) |
NOONAN SYNDROME 5 | (OMIM:611553) |
NOONAN SYNDROME 6 | (OMIM:613224) |
NOONAN SYNDROME 8 | (OMIM:615355) |
Neurofibromatosis - Noonan syndrome | (Orphanet:638) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Okamoto syndrome | (Orphanet:2729) |
Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES | (OMIM:602196) |
PTERYGIUM COLLI, ISOLATED | (OMIM:177990) |
Pachygyria - epilepsy - intellectual deficit - dysmorphism | (Orphanet:94084) |
Peters-plus syndrome | (Orphanet:709) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Pterygium colli - intellectual deficit - digital anomalies | (Orphanet:2988) |
SCARF syndrome | (Orphanet:3134) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Short stature - webbed neck - heart disease | (Orphanet:2865) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Split hand - urinary anomalies - spina bifida | (Orphanet:2437) |
Spondylo-ocular syndrome | (Orphanet:85194) |
Tetrasomy 12p | (Orphanet:884) |
Trisomy 18 | (Orphanet:3380) |
Turner syndrome | (Orphanet:881) |
Wildervanck syndrome | (Orphanet:3456) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked mandibulofacial dysostosis | (Orphanet:1131) |
Zunich-Kaye syndrome | (Orphanet:3474) |
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME | (OMIM:601321) |