Webbed neck

Symptom Information:

Symptom ID: HPO:0000465
Synonyms:
Pterygium colli [HPO:0000465]
Neck webbing [Orphanet:14300]
Neck webbing [HPO:0000465]
Neck webbing (disorder) [Orphanet:14300]
Pterygium colli [OMIM:Pterygium colli]
Webbed neck [OMIM:Webbed neck]
Webbed neck/pterygium colli [Orphanet:14300]
Pterygium colli [Orphanet:14300]
Pterygium colli [MedDRA:10051972]
Webbing of neck [MedDRA:10051972]
Webbed neck (1 patient) [OMIM:Webbed neck (1 patient)]
Webbed neck (in some patients) [OMIM:Webbed neck (in some patients)]
Webbed neck (rare) [OMIM:Webbed neck (rare)]
Quality:
Cross references:
Orphanet:14300 "Webbed neck/pterygium colli" [Orphanet:14300]
OMIM: "Pterygium colli" [OMIM:Pterygium colli]
OMIM: "Webbed neck" [OMIM:Webbed neck]
OMIM: "Webbed neck (1 patient)" [OMIM:Webbed neck (1 patient)]
OMIM: "Webbed neck (in some patients)" [OMIM:Webbed neck (in some patients)]
OMIM: "Webbed neck (rare)" [OMIM:Webbed neck (rare)]
UMLS:C0221217 "Neck webbing" [Orphanet:14300]
Is a (Direct Parents):
HPO         Abnormality of the neck
Orphanet Abnormality of the neck
MedDRA Musculoskeletal and connective tissue disorders of face, neck and jaw congenital
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)
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)