Fetal fifth finger clinodactyly
Symptom Information:
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Symptom ID:
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HPO:0011431
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Synonyms:
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| Fifth finger clinodactyly [Orphanet:20620] | | Clinodactyly of fifth finger [Orphanet:20620] | | Clinodactyly of fifth finger [OMIM:Clinodactyly of fifth finger] | | Clinodactyly of fifth fingers [OMIM:Clinodactyly of fifth fingers] | | Clinodactyly of fifth fingers (1/4 patients) [OMIM:Clinodactyly of fifth fingers (1/4 patients)] | | Clinodactyly of fifth fingers (in some patients) [OMIM:Clinodactyly of fifth fingers (in some patients)] | | Clinodactyly, fifth finger [OMIM:Clinodactyly, fifth finger] | | Clinodactyly, fifth finger (rare) [OMIM:Clinodactyly, fifth finger (rare)] | | Clinodactyly, fifth fingers [OMIM:Clinodactyly, fifth fingers] | | Fifth finger clinodactyly (female) [OMIM:Fifth finger clinodactyly (female)] | | Fifth finger clinodactyly (females) [OMIM:Fifth finger clinodactyly (females)] |
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Quality:
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Cross references:
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| HPO:0004209 "Clinodactyly of the 5th finger" [Orphanet:20620] | | Orphanet:20620 "Clinodactyly of fifth finger" [Orphanet:20620] | | OMIM: "Clinodactyly of fifth finger" [OMIM:Clinodactyly of fifth finger] | | OMIM: "Clinodactyly of fifth fingers" [OMIM:Clinodactyly of fifth fingers] | | OMIM: "Clinodactyly of fifth fingers (1/4 patients)" [OMIM:Clinodactyly of fifth fingers (1/4 patients)] | | OMIM: "Clinodactyly of fifth fingers (in some patients)" [OMIM:Clinodactyly of fifth fingers (in some patients)] | | OMIM: "Clinodactyly, fifth finger" [OMIM:Clinodactyly, fifth finger] | | OMIM: "Clinodactyly, fifth finger (rare)" [OMIM:Clinodactyly, fifth finger (rare)] | | OMIM: "Clinodactyly, fifth fingers" [OMIM:Clinodactyly, fifth fingers] | | OMIM: "Fifth finger clinodactyly (female)" [OMIM:Fifth finger clinodactyly (female)] | | OMIM: "Fifth finger clinodactyly (females)" [OMIM:Fifth finger clinodactyly (females)] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
All(HPO:0000001)
Phenotypic abnormality(HPO:0000118)
Abnormality of prenatal development or birth(HPO:0001197)
Fetal ultrasound soft marker(HPO:0011425)
Fetal fifth finger clinodactyly(HPO:0011431)
MedDRA:
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Database Frequency:
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14 / 7739
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Resource:
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All diseases associated with this symptom:
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17q12 microduplication syndrome
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(Orphanet:261272)
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48,XXYY syndrome
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(Orphanet:10)
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APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES
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(OMIM:300887)
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Absence of fingerprints - congenital milia
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(Orphanet:1658)
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Bloom syndrome
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(Orphanet:125)
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Cardiodysrhythmic potassium-sensitive periodic paralysis
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(Orphanet:37553)
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Craniofacial dysplasia-osteopenia syndrome
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(Orphanet:314555)
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Craniofrontonasal dysplasia
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(Orphanet:1520)
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HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES
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(OMIM:614684)
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Hennekam-Beemer syndrome
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(Orphanet:2135)
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Intellectual deficit, X-linked - craniofacioskeletal syndrome
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(Orphanet:163979)
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MEIER-GORLIN SYNDROME 3
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(OMIM:613803)
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MEIER-GORLIN SYNDROME 5
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(OMIM:613805)
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Microcephalic primordial dwarfism, Dauber type
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(Orphanet:319675)
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