Overfolded helix
Symptom Information:
Symptom ID: | HPO:0000396 | ||||||||||
Synonyms: |
|
||||||||||
Quality: | |||||||||||
Cross references: |
|
||||||||||
Is a (Direct Parents): |
|
||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the ear(HPO:0000598) Abnormality of the outer ear(HPO:0000356) Abnormality of the pinna(HPO:0000377) Abnormality of the helix(HPO:0011039) Abnormally folded helix(HPO:0008544) Overfolded helix(HPO:0000396) MedDRA: |
||||||||||
Database Frequency: | 21 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
BARAITSER-WINTER SYNDROME 1 | (OMIM:243310) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Down syndrome | (Orphanet:870) |
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES | (OMIM:614684) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Koolen-De Vries syndrome | (Orphanet:96169) |
MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA | (OMIM:608624) |
Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
Marshall-Smith syndrome | (Orphanet:561) |
Multiple congenital anomalies - hypotonia - seizures syndrome | (Orphanet:280633) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS | (OMIM:609654) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Zunich-Kaye syndrome | (Orphanet:3474) |