Plagiocephaly

Symptom Information:

Symptom ID: HPO:0001357
Synonyms:
Plagiocephaly (disorder) [Orphanet:2280]
Plagiocephaly [Orphanet:2280]
Plagiocephaly [OMIM:Plagiocephaly]
Plagiocephaly [MedDRA:10048586]
Plagiocephaly (1 patient) [OMIM:Plagiocephaly (1 patient)]
Plagiocephaly (asymmetry of orbits) [OMIM:Plagiocephaly (asymmetry of orbits)]
Plagiocephaly (in some patients) [OMIM:Plagiocephaly (in some patients)]
Quality:
Cross references:
Orphanet:2280 "Plagiocephaly" [Orphanet:2280]
OMIM: "Plagiocephaly" [OMIM:Plagiocephaly]
OMIM: "Plagiocephaly (1 patient)" [OMIM:Plagiocephaly (1 patient)]
OMIM: "Plagiocephaly (asymmetry of orbits)" [OMIM:Plagiocephaly (asymmetry of orbits)]
OMIM: "Plagiocephaly (in some patients)" [OMIM:Plagiocephaly (in some patients)]
UMLS:C0265529 "Plagiocephaly" [HPO:0001357]
UMLS:C0265529 "Plagiocephaly" [Orphanet:2280]
Is a (Direct Parents):
HPO         Abnormality of calvarial morphology
MedDRA Musculoskeletal and connective tissue disorders of skull congenital
Orphanet Craniosynostosis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the skull(HPO:0000929)
                Abnormality of the calvaria(HPO:0002683)
                   Abnormality of calvarial morphology(HPO:0002648)
                      Plagiocephaly(HPO:0001357)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of the calvaria(HPO:0002683)
                      Abnormality of calvarial morphology(HPO:0002648)
                         Plagiocephaly(HPO:0001357)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of skull congenital(MedDRA:10028382)
          Plagiocephaly(HPO:0001357)
Database Frequency: 106 / 7739
Resource:

All diseases associated with this symptom:

14q11.2 microdeletion syndrome (Orphanet:261120)
3C syndrome (Orphanet:7)
3q13 microdeletion syndrome (Orphanet:1621)
6q25 microdeletion syndrome (Orphanet:251056)
Achondroplasia (Orphanet:15)
Acrokeratoelastoidosis of Costa (Orphanet:38)
Acromegaly (Orphanet:963)
Acute intermittent porphyria (Orphanet:79276)
Aggressive systemic mastocytosis (Orphanet:98850)
Aicardi syndrome (Orphanet:50)
Aicardi-Goutières syndrome (Orphanet:51)
Alexander disease (Orphanet:58)
Anophthalmia - megalocornea - cardiopathy - skeletal anomalies (Orphanet:1101)
Auriculoocular anomalies - cleft lip (Orphanet:71270)
BRESEK syndrome (Orphanet:85284)
Babesiosis (Orphanet:108)
Beckwith-Wiedemann syndrome due to NSD1 mutation (Orphanet:238613)
Bird headed-dwarfism, Montreal type (Orphanet:2617)
Buerger disease (Orphanet:36258)
Böök syndrome (Orphanet:1262)
CHROMOSOME 15q11.2 DELETION SYNDROME (OMIM:615656)
Cabezas syndrome (Orphanet:85293)
Craniofrontonasal dysplasia (Orphanet:1520)
Cutis laxa (Orphanet:209)
Developmental delay with autism spectrum disorder and gait instability (Orphanet:329195)
Diencephalic syndrome (Orphanet:1672)
Dihydropyrimidinuria (Orphanet:38874)
Distomatosis (Orphanet:1685)
Dyskeratosis congenita (Orphanet:1775)
Eosinophilic granuloma (Orphanet:99871)
Epidermolytic palmoplantar keratoderma (Orphanet:2199)
Erdheim-Chester disease (Orphanet:35687)
Faciocardiorenal syndrome (Orphanet:1973)
Familial cold urticaria (Orphanet:47045)
Familial dysautonomia (Orphanet:1764)
Familial lambdoid synostosis (Orphanet:3267)
Familial thrombocytosis (Orphanet:71493)
Fetal brain disruption sequence (Orphanet:1665)
Fibrochondrogenesis (Orphanet:2021)
Fine-Lubinsky syndrome (Orphanet:1272)
Focal palmoplantar and gingival keratoderma (Orphanet:2200)
Follicular lymphoma (Orphanet:545)
Fucosidosis (Orphanet:349)
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type (Orphanet:79399)
Giant cell arteritis (Orphanet:397)
HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES (OMIM:236410)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 (OMIM:239300)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 (OMIM:614749)
Hereditary sensory and autonomic neuropathy type 2 (Orphanet:970)
Hirschsprung disease - ganglioneuroblastoma (Orphanet:2151)
Hodgkin lymphoma (Orphanet:98293)
Hodgkin lymphoma, classical (Orphanet:391)
Holoprosencephaly - craniosynostosis (Orphanet:2163)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
Hypertryptophanemia (Orphanet:2224)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit, X-linked - plagiocephaly (Orphanet:2898)
Isolated plagiocephaly (Orphanet:35098)
Joubert syndrome 1 (OMIM:213300)
Keratosis palmaris et plantaris - clinodactyly (Orphanet:86919)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Linear nevus sebaceus syndrome (Orphanet:2612)
Localized epidermolysis bullosa simplex (Orphanet:79400)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 (OMIM:614563)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 (OMIM:616268)
Mal de Meleda (Orphanet:87503)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Microgastria - limb reduction defect (Orphanet:2538)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies (Orphanet:369897)
Muenke syndrome (Orphanet:53271)
Nakajo-Nishimura syndrome (Orphanet:2615)
Naxos disease (Orphanet:34217)
Neurofaciodigitorenal syndrome (Orphanet:2673)
Nodular lymphocyte predominant Hodgkin lymphoma (Orphanet:86893)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Odontotrichomelic syndrome (Orphanet:2723)
Osteogenesis imperfecta (Orphanet:666)
Pachydermoperiostosis (Orphanet:2796)
Pachyonychia congenita (Orphanet:2309)
Palmoplantar keratoderma, Nagashima type (Orphanet:140966)
Peeling skin syndrome (Orphanet:817)
Pentasomy X (Orphanet:11)
Peripheral motor neuropathy - dysautonomia (Orphanet:2400)
Pitt-Hopkins-like syndrome 2 (OMIM:614325)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Primary cutaneous anaplastic large cell lymphoma (Orphanet:300865)
Primary cutaneous lymphoma (Orphanet:542)
ROBINOW-SORAUF SYNDROME (OMIM:180750)
Saethre-Chotzen syndrome (Orphanet:794)
Scrub typhus (Orphanet:83317)
Severe intellectual deficit - epilepsy - anal anomalies - distal phalangeal hypoplasia (Orphanet:94066)
Short stature - heart defect - craniofacial anomalies (Orphanet:1088)
Splenogonadal fusion - limb defects - micrognathia (Orphanet:2063)
Spontaneous periodic hypothermia (Orphanet:29822)
Stüve-Wiedemann syndrome (Orphanet:3206)
Summitt syndrome (Orphanet:3210)
Takayasu arteritis (Orphanet:3287)
Thymic carcinoma (Orphanet:99868)
Torticollis - keloids - cryptorchidism - renal dysplasia (Orphanet:3341)
Transgrediens et progrediens palmoplantar keratoderma (Orphanet:495)
Trisomy 20p (Orphanet:261318)
Tumoral calcinosis (Orphanet:53715)
Von Hippel-Lindau disease (Orphanet:892)