HP:0000006 | Autosomal dominant inheritance | "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators] |
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HP:0000007 | Autosomal recessive inheritance | "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators] |
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HP:0000232 | Everted lower lip | |
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HP:0000457 | Flat nose | |
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HP:0000535 | Sparse eyebrows | |
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HP:0000607 | Periorbital wrinkles | |
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HP:0000653 | Sparse eyelashes | "Decreased density/number of eyelashes." [pmid:19125427] |
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HP:0000668 | Hypodontia | "Hypodontia describes a situation when there are fewer than the normal number of teeth, whereby 6 teeth or fewer teeth are missing (oligodontia refers to the condition of missing more than 6 teeth and the congenital absence of all teeth is called anodontia)." [HPO:curators] |
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HP:0000674 | Anodontia | "The congenital absence of all teeth." [HPO:curators] |
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HP:0000685 | Hypoplastic teeth | |
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HP:0000691 | Microdontia | |
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HP:0000958 | Dry skin | |
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HP:0000963 | Thin skin | |
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HP:0000964 | Eczema | "Eczema is a form of dermatitis. The term eczema is broadly applied to a range of persistent skin conditions and can be related to a number of underlying conditions. Manifestations of eczema can include dryness and recurring skin rashes with redness, skin edema, itching and dryness, crusting, flaking, blistering, cracking, oozing, or bleeding." [HPO:curators] |
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HP:0000966 | Hypohidrosis | "Abnormally diminished capacity to sweat." [HPO:curators] |
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HP:0000968 | Ectodermal dysplasia | |
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HP:0000970 | Anhidrosis | "Inability to sweat." [HPO:curators] |
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HP:0001000 | Abnormality of skin pigmentation | |
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HP:0001006 | Hypotrichosis | "Reduced or lacking hair growth." [HPO:curators] |
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HP:0001106 | Periorbital hyperpigmentation | |
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HP:0001231 | Abnormality of the fingernails | "An abnormality of the `fingernails` (FMA:54327)." [HPO:probinson] |
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HP:0001425 | Heterogeneous | |
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HP:0001596 | Alopecia | "Loss of hair from the head or body." [HPO:curators] |
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HP:0002007 | Frontal bossing | "The presence of an unusually prominent forehead." [HPO:curators] |
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HP:0002046 | Intolerance to heat and fever | |
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HP:0002047 | Malignant hyperthermia | "Malignant hyperthermia is characterized by a rapid increase in temperature to 39-42 degrees C in response to inhalational anesthetics such as halothane or to muscle relaxants such as succinylcholine." [HPO:curators] |
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HP:0002164 | Nail dysplasia | |
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HP:0002213 | Fine hair | |
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HP:0002217 | Slow-growing hair | |
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HP:0002231 | Sparse body hair | "Sparseness of the body hair." [HPO:probinson] |
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HP:0005280 | Depressed nasal root and bridge | |
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HP:0006323 | Premature deciduous tooth loss | |
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HP:0006482 | Abnormality of dental morphology | |
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HP:0007607 | Hypohidrotic ectodermal dysplasia | |
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HP:0008388 | Abnormality of the toenails | |
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HP:0010803 | Everted upper lip vermilion | "Inner aspect of the upper lip vermilion (normally apposing the teeth) visible in a frontal view, i.e., the presence of an `everted` (PATO:0001597) `upper lip` (FMA:59817)." [HPO:probinson, pmid:19125428] |
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HP:0011220 | Prominent forehead | "Forward prominence of the entire forehead, due to protrusion of the frontal bone." [pmid:19125436] |
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HP:0012471 | Thick vermilion border | "Increased width of the "skin of vermilion border region of upper lip" (FMA:312645)." [HPO:probinson] |
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