Plagiocephaly
Symptom Information:
Symptom ID: | HPO:0001357 | |||||||
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 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) 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) 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) |
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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) |